| Symbol | ABT |
|---|---|
| Name | ABBOTT LABORATORIES |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 100 ABBOTT PARK ROAD, ABBOTT PARK, Illinois, 60064-6400, United States |
| Telephone | +1 224 667-6100 |
| Fax | — |
| — | |
| Website | https://www.abbottinvestor.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0000001800 |
| Description | Abbott manufactures and markets medical devices, adult and pediatric nutritional products, diagnostic equipment and testing kits, and branded generic drugs. Products include pacemakers, implantable cardioverter defibrillators, neuromodulation devices, coronary stents, catheters, infant formula, nutritional liquids for adults, molecular diagnostic platforms, and immunoassays and point-of-care diagnostic equipment. Abbott derives approximately 60% of sales outside the United States. Additional info from NASDAQ: |
(93% Neutral) ABBOTT LABORATORIES (ABT) Reports Q3 2026 Financial Results
Read moreAbbott Reports Second-Quarter 2026 Results and Raises Full-Year EPS Guidance
Read moreCushman Elizabeth C. 🔴 sold 560 shares of ABBOTT LABORATORIES (ABT) at $94.12 Transaction Date: Jun 27, 2026 | Filing ID: 000009
Read moreNew research shows even stronger health outcomes for participants in a Food is Medicine program when paired with support from community health workers
Read moreNew Abbott data show many people with diabetes may not recognize symptoms of diabetic ketoacidosis
Read moreNew Form SD - ABBOTT LABORATORIES <b>Filed:</b> 2026-05-27 <b>AccNo:</b> 0001104659-26-066986 <b>Size:</b> 52 KB
Read moreAbbott secures CE Mark for worlds first dual glucose-ketone sensing technology for people with diabetes
Read moreACS guideline reaffirms Abbott leadership in noninvasive colorectal cancer screening
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00000644 | A Phase II Safety and Efficacy Study of Clarithromycin in the Treatment of Diss… | Phase2 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00002275 | A Comparison of Two Types of Injected Nutritional Supplements in Patients With … | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002366 | The Safety and Effectiveness of Ritonavir in the Treatment of HIV-Related Kapos… | Phase2 | Sarcoma, Kaposi | Completed | — | — | ClinicalTrials.gov |
| NCT00004580 | A Study of ABT-378/Ritonavir Combination in HIV-Infected Patients Who Have Take… | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00004581 | A Study to Compare Two Anti-HIV Drug Combinations in HIV-Infected Patients Who … | Phase3 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT06321705 | Safety and Efficacy of Continued CS1 Treatment of Patients With Pulmonary Arter… | — | Pulmonary Arterial Hypertension | Available | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT01078610 | Safety and Effectiveness and Effect on Quality of Life and Work Productivity of… | — | Psoriatic Arthritis | Withdrawn | — | — | ClinicalTrials.gov |
| NCT01144156 | Small Bowel Mucosal Healing Induced by Adalimumab in Crohn's Disease Patients a… | Na | Crohn's Disease | Unknown | — | — | ClinicalTrials.gov |
| NCT00121017 | A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Susti… | Phase2 | HIV Infection | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00583401 | PFO ACCESS Registry | — | Patent Foramen Ovale | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00583505 | Emergency/Compassionate Use - Membranous VSD Occluder | — | Membranous | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00584064 | Emergency/Compassionate Use PFO Occluder | — | Patent Foramen Ovale | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00590382 | Emergency/Compassionate Use - Muscular VSD Occluder | — | Muscular | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00002036 | Phase I Safety Study of Anti-HIV Immune Serum Globulin (Human) | Phase1 | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002029 | Long-Term Nutritional Support in Patients With the Acquired Immunodeficiency Sy… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00650026 | Early Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalim… | — | Rheumatoid Arthritis | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT00002201 | A Study of Ritonavir (ABT-538) When Used With Nelfinavir in HIV-Infected Patien… | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00002223 | A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients | Na | HIV Infections | Completed | — | — | ClinicalTrials.gov |
| NCT00000971 | The Safety and Effectiveness of Clarithromycin Plus Zidovudine or Dideoxyinosin… | Phase1 | Mycobacterium Avium-intracellulare Infection | Completed | — | — | ClinicalTrials.gov |
| NCT00000961 | The Safety and Effectiveness of Hyperimmune Anti-HIV Intravenous Immunoglobulin… | Phase2 | HIV Infections | Terminated | — | — | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07696182 | Validation Of anatomY-specific Aortic Valve Implantation Guided by Software Usi… | Na | Severe Native Calcific Aortic Stenosis | Not_Yet_Recruiting | 2026-11-30 | 2038-12-30 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07666581 | Influence of the Use of Specific Nutritional Formulas on Time in Range in Patie… | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2026-08-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07270562 | ORbital Atherectomy for Lesion Preparation in Patients With Chronic Limb-threat… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT07270575 | REsorbable SCaffolds With everolimUs-Elution for the Treatment of Infrapoplitea… | — | Chronic Limb Threatening Ischemia | Not_Yet_Recruiting | 2026-08-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07626658 | Food-i-Sense Analytics: Integrating AI Into Continuous Glucose Monitoring Data … | — | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | Not_Yet_Recruiting | 2026-07-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT07621003 | PULSed Field Ablation for Atrial Fibrillation Using a Balloon for Early Interve… | Na | Atrial Fibrillation | Not_Yet_Recruiting | 2026-07-01 | 2031-03-31 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07211802 | CKM For Safe Use of SGLT2i in Type 1 Diabetes | Phase3 | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-07-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07586995 | A Post-Market Assessment of the Safety and Performance of the TriClip™ System | — | Tricuspid Regurgitation (TR) | Recruiting | 2026-06-01 | 2033-08-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07524907 | Stunting and Targeting Reduction of Impaired Growth in Kids Effectively | — | Malnutrition (Calorie) | Not_Yet_Recruiting | 2026-06-01 | 2028-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07599982 | Safety Evaluation of MODI, an Insulin Titration Algorithm, in Adults With Diabe… | Na | Type 1 Diabetes (T1D) | Recruiting | 2026-05-25 | 2027-01-01 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07638995 | Single Chamber Atrial Leadless Pacing for Isolated Sinus Node Dysfunction | — | Atrial Fibrillation | Recruiting | 2026-05-18 | 2029-12-31 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07604844 | Comparative Efficacy of Intralesional Tranexamic Acid Versus Mandelic Acid Peel… | Na | Melasma | Not_Yet_Recruiting | 2026-05-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07421076 | Grid eXplore Mapping Study | Na | Paroxysmal Atrial Fibrillation (PAF) | Recruiting | 2026-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07045298 | CGM Use in Heart Failure | Na | Heart Failure | Not_Yet_Recruiting | 2026-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07423637 | The Impact of Early Automated Insulin Delivery (AID) Therapy on Diabetes Contro… | Na | Type 1 Diabetes | Not_Yet_Recruiting | 2026-04-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-31 | 2028-02-28 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT07441382 | Catheter Ablation Plus LAAO Versus Anticoagulation in Frail Elderly Patients Wi… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-03-24 | 2028-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT04823299 | Randomized Controlled Trial- Ablation Strategy for Paroxysmal Atrial Fibrillati… | Na | Atrial Fibrillation | Recruiting | 2026-03-23 | 2030-03-01 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07426406 | Oral Nutritional Supplement in Adults With or at Risk of Malnutrition | Na | Gastrointestinal Tolerance | Completed | 2026-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07509658 | TriClip Japan Post-Approval Study | — | Tricuspid Regurgitation | Recruiting | 2026-03-02 | 2029-12-15 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07135531 | Continuous Glucose Monitoring (CGM) in an Underserved Population | Na | Diabetes | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Na | Cardiac Arrythmias | Recruiting | 2026-02-16 | 2026-08-03 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07331792 | Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Tre… | Phase1 | Pityriasis Versicolor | Not_Yet_Recruiting | 2026-02-02 | 2026-05-31 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07256925 | Malnutrition Screening Study | — | Malnutrition, Calorie | Recruiting | 2026-01-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07271043 | Nutrition+: Effect of a High-Protein Diabetes Formula on Body Composition in Ty… | Na | Type 2 Diabetes | Recruiting | 2026-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Na | Ischemic Heart Disease (IHD) | Recruiting | 2025-12-17 | 2031-10-31 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07250828 | Efficacy and Feasibility of BurstDR SCS in Painful Diabetic Neuropathy | Na | Painful Diabetic Neuropathy (PDN) | Enrolling_By_Invitation | 2025-12-15 | 2027-05-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07287423 | LEAP 2 Chronic EFS | Na | Cardiac Pacemaker | Recruiting | 2025-12-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Na | Paroxysmal AF | Recruiting | 2025-12-11 | 2027-08-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07240012 | Automated Insulin Delivery Versus Usual Insulin Treatment Modality Before and D… | Na | Diabete Type 1 | Recruiting | 2025-12-01 | 2028-10-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07422688 | Optical Coherence Tomography in Acute Vessel Evaluation | Na | Ischemic Heart Disease | Enrolling_By_Invitation | 2025-11-23 | 2039-09-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07193888 | Navitor Japan Study | — | Severe Aortic Stenosis | Recruiting | 2025-10-30 | 2028-08-01 | ClinicalTrials.gov |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System f… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2025-10-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07359898 | International Multicenter Study of the Navitor/Navitor Vision Transcatheter Aor… | — | Severe Native Aortic Stenosis | Recruiting | 2025-10-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07215104 | A Prospective Evaluation of Spinal Cord Induced Muscle Stimulation (MuscleSCS) … | Na | Chronic Low Back Pain (CLBP) | Recruiting | 2025-10-07 | 2027-01-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07203183 | Dengue - Sample Collection Study Pakistan | — | Dengue | Not_Yet_Recruiting | 2025-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07198529 | OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in S… | Na | Stable Angina | Recruiting | 2025-09-30 | 2029-09-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287618 | Evaluation of Potassium (K) and Ionized Calcium (iCa) Tests Using Capillary Spe… | Na | Hematologic Tests | Recruiting | 2025-09-17 | 2026-12-01 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06014242 | Peripheral Microvascular Resistance as a Predictor for Limb Salvage | Na | Peripheral Arterial Disease | Withdrawn | 2025-09-15 | 2026-09-15 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT06743204 | The Integrated Female Sexually Transmitted Infection Testing for HIV Epidemic C… | Na | Gonorrhea Female | Recruiting | 2025-09-08 | 2029-01-31 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07157384 | REMIssion of Type 2 Diabetes Between Intermittently Scanned Continuous Glucose … | Na | Type 2 Diabetes | Not_Yet_Recruiting | 2025-09-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | — | Mitral Regurgitation | Recruiting | 2025-08-13 | 2028-12-01 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Na | Bradycardia | Recruiting | 2025-07-24 | 2027-04-30 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06920745 | TriClip CED RWE Study | — | Tricuspid Regurgitation | Recruiting | 2025-07-08 | 2032-07-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT06928129 | Clinical Feasibility of the BinaxNOW™ COVID-19/Flu A&B Combo in the Southern He… | Na | Influenza Type A | Not_Yet_Recruiting | 2025-06-30 | 2025-11-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT07244939 | Cephea South America Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06736665 | Orbital Atherectomy vs Intravascular Lithotripsy for the Treatment of Calcified… | Na | Coronary Arterial Disease (CAD) | Recruiting | 2025-06-12 | 2027-12-01 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06733324 | RCT of SCERTS (Social Communication, Emotional Regulation, Transactional Suppor… | Na | Autism Spectrum Disorder (ASD | Active_Not_Recruiting | 2025-06-01 | 2026-12-15 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06932588 | Biomarker Role in Assessing Imaging Needs for Mild Cranial Trauma | Na | Brain Injuries | Recruiting | 2025-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06795035 | Assessment of Coronary Microvascular Dysfunction After STEMI Using Continuous S… | — | ST Elevation Myocardial Infarction | Recruiting | 2025-05-29 | 2027-12-31 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT06957028 | CGM for the Early Detection and Management of Hyperglycemia in Pregnancy | Na | Gestational Diabetes Mellitus in Pregnancy | Recruiting | 2025-05-27 | 2027-11-27 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | — | Leadless Pacemaker | Recruiting | 2025-05-26 | 2029-11-01 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06888687 | Comparison of Dietetics Support With and Without Continuous Glucose Monitoring … | Na | Type 2 Diabetes Mellitus (T2DM) | Active_Not_Recruiting | 2025-05-12 | 2026-11-28 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06959797 | Insulin Pump Versus Full Closed-loop for Type 2 Diabetes | Na | Type 2 Diabetes | Recruiting | 2025-05-05 | 2028-12-31 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06815536 | Master Protocol for Evaluating Multiple Infection Diagnostics for Ciprofloxacin… | — | Neisseria Gonorrheae Infection | Recruiting | 2025-04-16 | 2026-07-01 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06931821 | Functional ElectroAnatomiC Isochronal Late Activation Mapping for Empiric VT Ab… | Na | Sustained Monomorphic VT (MMVT) | Not_Yet_Recruiting | 2025-04-15 | 2029-04-30 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06830746 | ASCEND CSP IDE Study | Na | Heart Failure | Active_Not_Recruiting | 2025-04-11 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06883864 | Efficacy and Safety of Catheter abLation in patiEnts With seVere mitrAl regurgi… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-08 | 2028-05-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06885177 | TECTONIC CAD IVL IDE Study | Na | Coronary Artery Calcification | Active_Not_Recruiting | 2025-04-01 | 2028-06-01 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06952296 | Study of the Effectiveness of Dydrogesterone in the Treatment of Endometriosis-… | — | Endometriosis | Not_Yet_Recruiting | 2025-04-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT07114393 | Optimization of Complex Percutaneous Coronary Intervention With Liberal Use of … | — | Coronary Artery Disease | Recruiting | 2025-04-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT04977310 | TARGET-LOAD Pilot Study Comparing Hemodynamics-guided LVAD Unloading Vs. Standa… | Na | Heart Failure | Withdrawn | 2025-03-31 | 2026-09-01 | ClinicalTrials.gov |
| NCT06902922 | Impact of Severe Tricuspid Regurgitation Correction on Gut Microbiota and Gastr… | — | Tricuspid Regurgitation (TR) | Not_Yet_Recruiting | 2025-03-31 | 2027-09-30 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06921902 | Glycemic Metrics and Patterns in People With and Without Prediabetes | — | Pre Diabetes | Recruiting | 2025-02-28 | 2026-12-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | — | Heart Failure | Recruiting | 2025-02-07 | 2032-03-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06766435 | Evaluation of the Abbott i-STAT TBI Biomarker Test | Na | Traumatic Brain Injury | Recruiting | 2025-01-30 | 2025-10-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06632002 | Diabetes-specific Formulas on Nutritional Outcomes in Individuals With Diabetes… | Na | Diabetes | Active_Not_Recruiting | 2025-01-02 | 2026-05-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06241430 | The CardioClip Study | Na | Heart Failure With Reduced Ejection Fraction | Recruiting | 2024-12-18 | 2030-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | — | Cardiac Arrhythmias | Recruiting | 2024-12-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in… | Na | Heart Failure | Recruiting | 2024-12-13 | 2032-09-01 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06709001 | An Observational Study to Assess Malnutrition Risk | — | Malnutrition | Completed | 2024-12-09 | 2025-07-25 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06492018 | Lay User Evaluation of the Panbio™ HCV Self Test in an EU Population | — | Hepatitis C | Not_Yet_Recruiting | 2024-12-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06676072 | A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PA… | Na | Atrial Fibrillation (AF) | Completed | 2024-11-22 | 2026-04-13 | ClinicalTrials.gov |
| NCT06669637 | Amplify EP Registry | — | Atrial Fibrillation | Not_Yet_Recruiting | 2024-11-22 | 2026-12-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT07082426 | Early System Experience With the Abbott Balloon-expandable TAVI System: First-I… | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2024-11-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06707688 | Abbott Medical - VERITAS Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2024-11-07 | 2027-09-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06668935 | Prolongation of GLP-1 Adherence When Using Continuous Glucose Monitoring | — | Diabetes Mellitus | Recruiting | 2024-10-24 | 2027-01-01 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06656364 | Esprit BTK Post-Approval Study | Na | Chronic Limb-Threatening Ischemia | Active_Not_Recruiting | 2024-10-21 | 2029-05-30 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06605573 | Lay User Evaluation of the Panbio™ HCV Self-Test | Na | HEPATITIS C (HCV) | Not_Yet_Recruiting | 2024-10-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06456541 | Infant Formula in Infants and Children With Cow's Milk Allergy | Na | Cow's Milk Allergy | Recruiting | 2024-10-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Na | Treatment Resistant Depression | Recruiting | 2024-09-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06790472 | Metabolic Wellness and CGM | — | Cardiometabolic Risk Factors | Enrolling_By_Invitation | 2024-09-05 | 2025-10-11 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06584214 | Evaluation of the Diagnostic Sensitivity and Specificity of the Determine™ Syph… | Na | Syphilis Infection | Not_Yet_Recruiting | 2024-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06590467 | Abbott Structural Heart Device Registry | — | Heart Diseases | Recruiting | 2024-08-21 | 2039-11-01 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06271967 | FOCALFLEX (CE Mark) Study | Na | Atrial Fibrillation Paroxysmal | Completed | 2024-08-15 | 2026-01-19 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06340763 | JETi Hong Kong Post Market Study (PMS) | — | Peripheral Venous Thrombosis | Completed | 2024-08-07 | 2025-02-15 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06395675 | Clinical Evaluation of the ID NOW™ CT/NG Test | Na | Chlamydia Trachomatis Infection | Unknown | 2024-07-09 | 2025-01-09 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06368765 | Oral Rehydration Solution and Dehydration Recovery | Na | Dehydration | Terminated | 2024-07-08 | 2024-10-17 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06434779 | Investigating Efficacy and Safety of JETi® in Arterial Occlusions in FEM-POP an… | Na | Peripheral Arterial Disease | Not_Yet_Recruiting | 2024-07-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06542133 | AVEIR Remote Care System Non-Significant Risk Study | — | Cardiac Pacemaker | Completed | 2024-06-10 | 2024-08-30 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06295835 | Method Comparison Study for Measuring Potassium (K) and Ionized Calcium (iCa) i… | Na | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | Completed | 2024-05-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06205537 | Muscle Health and Recovery in Older Adults | Na | Exercise Induced Muscle Damage | Completed | 2024-05-20 | 2025-08-19 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06436053 | Acute Response to Left Bundle Branch Area Pacing With SyncAV | — | Heart Failure | Recruiting | 2024-05-15 | 2027-07-15 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06375590 | NavIIcusp: Bicuspid Aortic Valve Stenosis With Navitor Platform International E… | — | Bicuspid Aortic Valve | Not_Yet_Recruiting | 2024-05-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT06268821 | Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated… | Na | Type 2 Diabetes Treated With Insulin | Terminated | 2024-04-02 | 2024-07-12 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT06266702 | Evaluation of a Nutritional Technology for Vitamin D Absorption | Na | Nutrition, Healthy | Completed | 2024-03-15 | 2024-05-02 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT05932615 | ENVISION IDE Trial: Safety and Effectiveness of NAVITOR in Transcatheter Aortic… | Na | Aortic Valve Stenosis | Enrolling_By_Invitation | 2024-03-15 | 2036-04-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06393478 | Southeastern Europe Microcirculation Registry | — | Angina, Microvascular | Recruiting | 2024-03-01 | 2034-03-01 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06217393 | Trial of Itopride 150mg Once a Day Versus Itopride 50 mg Thrice a Day; in Patie… | Phase3 | Functional Dyspepsia | Completed | 2024-02-28 | 2025-02-28 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06262295 | A Safety and Effectiveness Monitoring in France for AVEIR VR LP and AVEIR AR LP… | — | Pacemaker | Recruiting | 2024-02-14 | 2029-09-01 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT06189365 | Amplatzer Amulet China Post Market Study (PMS) | — | Non-Valvular Atrial Fibrillation | Terminated | 2024-01-30 | 2025-12-05 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT07271433 | Continuous Glucose Monitoring for Post-kidney Transplantation in Pre-existing T… | — | Kidney Transplant | Completed | 2024-01-29 | 2026-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT06100770 | Aveir AR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2024-01-18 | 2031-01-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT05758805 | Esophageal Injury of a Tip CF Sensing Ablation Catheter for HP-SD of Paroxysmal… | Na | Atrial Fibrillation | Recruiting | 2024-01-08 | 2025-10-01 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06356727 | Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remode… | Na | Heart Failure | Recruiting | 2024-01-03 | 2030-01-31 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT06172699 | Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study | — | Atrial Fibrillation Paroxysmal | Completed | 2024-01-01 | 2025-11-10 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT05913193 | Oral Nutritional Supplement in Type 2 Diabetes Subjects With or at Risk of Maln… | — | Malnutrition | Completed | 2023-12-15 | 2025-06-17 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT07382076 | Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population | — | Activated Clotting Time | Active_Not_Recruiting | 2023-12-15 | 2026-03-30 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT06124638 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel to Support Home Use | Na | COVID-19 | Completed | 2023-12-04 | 2024-04-03 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT05981547 | Patterns and Glycaemic Endpoints for Diagnosing Gestational Diabetes | — | Gestational Diabetes | Active_Not_Recruiting | 2023-11-22 | 2026-06-21 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT06127108 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Panel | Na | COVID-19 | Completed | 2023-11-14 | 2024-02-02 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-12-31 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT05932602 | AVEIR DR Coverage With Evidence Development (CED) Study | — | Cardiac Pacemaker | Recruiting | 2023-10-31 | 2030-05-01 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06039176 | Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future | — | LVAD | Recruiting | 2023-10-27 | 2026-12-30 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06106594 | VOLT CE Mark Study | Na | Atrial Arrhythmia | Recruiting | 2023-10-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06025994 | Standardizing the Management of Patients With Coronary Microvascular Dysfunction | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-10-10 | 2029-02-10 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT06008080 | Post-Market Clinical Follow Up Study With Navitor Valve | — | Aortic Stenosis | Recruiting | 2023-09-29 | 2032-06-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05877612 | Efficacy of Spinal Cord Stimulation in Burst Mode in the Treatment of Complex R… | — | Complex Regional Pain Syndrome Type I | Unknown | 2023-09-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05572034 | Cardiac Autonomic Denervation for Cardio-inhibitory Syncope | Na | Bradycardia; Syncope | Unknown | 2023-09-01 | 2024-03-30 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05705427 | The COMBAT HBV Feasibility Trial | Phase4 | Hepatitis B | Completed | 2023-08-17 | 2025-11-25 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05839873 | Abbott Ventricular Tachycardia PAS | — | Ventricular Tachycardia | Active_Not_Recruiting | 2023-07-24 | 2026-11-01 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05944432 | CGM Use in Adults With Type 2 Diabetes on Basal Insulin | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2023-07-14 | 2027-11-30 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05387954 | PFO Closure, Oral Anticoagulants or Antiplatelet Therapy After PFO-associated S… | Phase3 | Cryptogenic Ischemic Stroke | Recruiting | 2023-07-07 | 2031-07-07 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05802927 | Diabetes-specific Formula (DSF) in Individuals With Type 2 Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2023-07-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05847283 | DPOS Versus GnRH Antagonist Protocol for Oocyte Accumulation in Low Ovarian Res… | Na | Diminished Ovarian Reserve | Recruiting | 2023-06-22 | 2027-12-31 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05537662 | External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO) | Na | Chronic Pain | Recruiting | 2023-06-06 | 2025-04-01 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05754775 | Remission of Type 2 Diabetes Via Calorie Restriction | Na | Type 2 Diabetes | Completed | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT05324683 | ILUMIEN-V - AERO: All-comEr Registry of OCT (AERO) | — | Myocardial Ischemia | Active_Not_Recruiting | 2023-05-04 | 2026-04-01 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06159231 | FAME II-10-year Follow-Up | — | Coronary Artery Disease | Completed | 2023-04-25 | 2024-05-15 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT06030284 | The True Efficacy of Burst Spinal Cord Stimulation in the Management of Intract… | Na | Chronic Intractable Pain | Withdrawn | 2023-04-20 | 2023-06-01 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05695716 | CSI Percutaneous Ventricular Assist Device (pVAD) Second in Human Study | Na | Coronary Artery Disease | Withdrawn | 2023-04-05 | 2023-07-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05833581 | Consistently Assess Signs and Symptom of Heart Failure | Na | Heart Failure | Unknown | 2023-03-17 | 2024-06-17 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05284955 | Screening for Advanced Heart Failure IN Stable outPatientS - The SAINTS Study (… | Phase4 | Advanced Heart Failure | Unknown | 2023-03-02 | 2025-12-31 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05715684 | Patient-Centered Surgical Prehabilitation | Na | Bladder Cancer | Recruiting | 2023-03-01 | 2027-12-25 | ClinicalTrials.gov |
| NCT05709795 | CTI Ablation Guided by Omnipolar Wave Speed and Voltage Maps to Diminish RF and… | Na | Flutter | Recruiting | 2023-03-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT05547165 | Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low … | Na | Ductus Arteriosus, Patent | Recruiting | 2023-02-21 | 2026-02-28 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT04818645 | Insertable Cardiac Monitor for Primary Atrial Fibrillation Detection in High-Ri… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2023-01-31 | 2028-07-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05599061 | Treatment of Functionally Non-significant Vulnerable Plaques in Patients With M… | Na | Coronary Artery Disease | Active_Not_Recruiting | 2023-01-30 | 2028-12-01 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05962710 | FreeStyle Libre 3 Continuous Glucose Monitoring System | — | Diabetes Mellitus | Terminated | 2023-01-27 | 2023-01-31 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05455489 | GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation With the… | — | Mitral Valve Regurgitation | Recruiting | 2023-01-25 | 2029-08-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05525039 | RCT of Combination Effect of Vibration Treatment and HMB Supplementation on Myo… | Na | Sarcopenia | Recruiting | 2023-01-12 | 2025-09-01 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05843461 | PIMR and Pulmonary Vascular Disease | — | Pulmonary Hypertension | Completed | 2023-01-10 | 2024-07-31 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT05529472 | Safety and Effectiveness Evaluation of Peripheral Orbital Atherectomy | Na | Peripheral Artery Disease | Completed | 2023-01-10 | 2024-10-10 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT05630365 | Clinical Evaluation of the Panbio™ COVID-19/Flu A&B Rapid Panel Professional Us… | Na | COVID-19 | Completed | 2022-12-15 | 2023-03-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT06306573 | CardioMEMS HF System Real-World Evidence Post-Approval Study | — | Heart Failure NYHA Class II | Enrolling_By_Invitation | 2022-12-15 | 2029-12-31 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05072730 | ComparIson of Strategies to PrepAre SeveRely CALCified Coronary Lesions 2 | Na | Calcified Coronary Artery Disease | Unknown | 2022-12-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05569044 | Oral Rehydration Solutions in Healthy Adult Athletes | Na | Hydration | Terminated | 2022-11-21 | 2024-06-18 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05437068 | Nutritional Supplementation in Children at Risk of Undernutrition | Na | Malnutrition, Child | Withdrawn | 2022-11-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05236153 | Electroanatomic Interactions Between Transcatheter Pulmonary Valve Prostheses a… | Na | Tetralogy of Fallot | Recruiting | 2022-11-04 | 2024-01-01 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05629572 | Abbott i-STAT High Sensitivity Troponin I Study | — | Myocardial Infarction | Completed | 2022-11-02 | 2024-03-11 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05897112 | Comparative Efficacy of 10% Potassium Hydroxide Solution Versus Cryotherapy in … | Phase1 | Molluscum Contagiosum | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05493904 | PREcise Percutaneous Coronary Intervention for Stent OptimizatION in Treatment … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2022-11-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05580978 | CGM Plus GEM in Prediabetes | Na | PreDiabetes | Completed | 2022-11-01 | 2025-01-15 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05884151 | Comparison of Intralesional Tranexamic Acid and Platelets Rich Plasma in the Tr… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05887219 | Comparison of Azelaic Acid 20 % Cream Versus Hydroquinone 4% Cream as an Adjuva… | Phase1 | Melasma | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05895071 | Comparison of Topical 5%Potassium Hydroxide vs Liquid Nitrogen in the Treatment… | Phase1 | Plan Warts | Completed | 2022-11-01 | 2023-04-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05434650 | Abbott Atrial Fibrillation Post Approval Study | — | Atrial Arrhythmia | Active_Not_Recruiting | 2022-10-21 | 2026-11-30 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05687591 | Left Atrial Appendage Occlusion With The Amplatzer Amulet Device: The Southeast… | — | Atrial Fibrillation | Completed | 2022-10-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05483140 | Digitally-Enabled Weight Management Program on T2DM | — | Weight Change, Body | Completed | 2022-09-30 | 2024-09-30 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05544864 | Intracoronary Stenting and Restenosis - Randomized Trial of Drug-eluting Stent … | Na | Coronary Artery Disease | Recruiting | 2022-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05261906 | The FreeStyle Libre Enabled Reduction of A1c Through Effective Eating and Exerc… | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2022-09-26 | 2025-10-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05655910 | Enhanced Nutritional Optimization in LVAD Trial | Na | Heart Failure | Recruiting | 2022-09-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT05516797 | IGNITE (Impact of Glucose moNitoring and nutrItion on Time in rangE) | Na | Type 2 Diabetes | Completed | 2022-09-22 | 2024-03-01 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05423379 | XIENCE Skypoint Large Vessel Post Approval Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2027-08-30 | ClinicalTrials.gov |
| NCT05288361 | The DISCOVER INOCA Prospective Multi-center Registry | — | Ischemia and No Obstructive Coronary Artery Disease | Active_Not_Recruiting | 2022-09-14 | 2032-12-31 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05428384 | Validation of CardioMEMS HF System Cardiac Output Algorithm IDE | — | Heart Failure | Completed | 2022-08-31 | 2024-01-30 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05822232 | FreeStyle Libre 2 Discharge Trial | Na | Diabetes Mellitus, Type 2 | Unknown | 2022-08-17 | 2024-04-30 | ClinicalTrials.gov |
| NCT05389631 | Trifecta and Epic ViV Detailed Insights Into Management Strategies and Outcomes | — | Aortic Valve Disease | Completed | 2022-08-17 | 2023-12-21 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT07059598 | Relationship of Nutritional Status to Chemotherapy Treatment Completion and Out… | — | Cancer-related Malnutrition | Completed | 2022-08-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05073419 | Arrhythmia Detection After MI | Na | Acute Myocardial Infarction | Recruiting | 2022-08-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05708131 | Outcomes of Functional Substrate Mapping of Ventricular Tachycardia | — | Ventricular Tachycardia | Unknown | 2022-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05752435 | Comparison of Therapeutic Efficacy Between Intralesional Bleomycin and Cryother… | Na | Viral Wart | Completed | 2022-07-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05301556 | Food for Special Medical Purpose in Patients With Digestive Tract Tumor | Na | Gastrointestinal Cancer | Completed | 2022-06-24 | 2024-01-09 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05336877 | Aveir VR Coverage With Evidence Development Post-Approval Study | — | Cardiac Pacemaker | Recruiting | 2022-06-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05270499 | Aveir VR Real-World Evidence Post-Approval Study | — | Cardiac Pacemaker | Active_Not_Recruiting | 2022-06-21 | 2034-09-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05712837 | Efficacy of 25% Trichloroacetic Acid Peel Versus 30% Salicylic Acid Peel in Mil… | Na | Acne Vulgaris | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05712811 | Comparison of Cryotherapy and Peeling Agent in the Treatment of Common Warts | Na | Warts | Completed | 2022-06-01 | 2022-11-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05344313 | Oral Nutritional Supplementation With HMB Enhance Muscle Quality in Sarcopenic … | Na | Sarcopenia | Completed | 2022-06-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05368454 | Evaluation of a Digital Diabetes Self-Management Education and Support Program | Na | Type 2 Diabetes | Completed | 2022-05-31 | 2024-01-24 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05326828 | Implantable Cardiac Monitor to Detect Atrial Fibrillation in Patients With MINO… | — | MINOCA | Recruiting | 2022-05-24 | 2031-05-15 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05286359 | Performance Evaluation of Malaria Plus Rapid Diagnostic Tests (RDTs) for the De… | Na | Malaria | Completed | 2022-05-24 | 2022-11-17 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05739786 | Comparisom of Liquid Nitrogen and Vitamin D3 in The Treatment of Cutaneous Warts | Phase1 | Cutaneous Warts | Completed | 2022-05-11 | 2022-11-11 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05369494 | Infants Fed a Hydrolyzed Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2022-05-07 | 2023-11-18 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05061004 | Cephea Early Feasibility Study | Na | Mitral Regurgitation | Recruiting | 2022-04-28 | 2031-03-01 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05370703 | A Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and … | — | Dyslipidemia | Completed | 2022-04-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05154045 | Postprandial Glycemic Response in Adults With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-04-09 | 2022-07-12 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05330468 | Regent China Post-Market Clinical Follow-up Study | — | Valvular Heart Disease | Completed | 2022-03-29 | 2024-10-10 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05327101 | Patient Preferences for Leadless Pacemakers | — | Cardiac Rhythm Disorder | Completed | 2022-03-28 | 2023-06-13 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05269862 | Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation | Na | Parkinson Disease | Active_Not_Recruiting | 2022-03-24 | 2024-12-01 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05333068 | COMBINE-INTERVENE: COMBINEd Ischemia and Vulnerable Plaque Percutaneous INTERVE… | Na | Multivessel Coronary Artery Disease | Active_Not_Recruiting | 2022-03-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05315544 | Cardiovascular Systems Inc. (CSI) pVAD First in Human Study | Na | Coronary Artery Disease | Completed | 2022-03-14 | 2022-03-16 | ClinicalTrials.gov |
| NCT05354115 | Sample Collection for Evaluation of the Panbio™ COVID-19/ Flu A&B Rapid Panel. | Na | COVID-19 | Completed | 2022-03-14 | 2022-08-22 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05057637 | The Impact of Optical Coherence Tomography on the Endovascular Treatment Planni… | — | Femoropopliteal Stenosis | Active_Not_Recruiting | 2022-03-09 | 2027-04-01 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05578950 | Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuou… | Phase1 | Onychomycosis | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05588999 | Comparative Study Between Treatment With Cryotherapy Alone Versus Cryotherapy P… | Phase1 | Plantar Wart | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05634460 | Comparison of 5% Potassium Hydroxide With 10% Potassium Hydroxide Solution in T… | Phase1 | Molluscum Contagiosum | Completed | 2022-03-01 | 2022-08-31 | ClinicalTrials.gov |
| NCT05862714 | Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Pati… | Phase1 | Tinea Versicolor | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05862701 | Comparison of Topical 5% Permethrin and Topical 10% Sulfur in the Treatment of … | Phase1 | Scabies | Completed | 2022-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05165693 | Evaluation of Glycemic Response in Individuals With Type 2 Diabetes | Na | Glycemic Control | Completed | 2022-02-23 | 2022-06-16 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05734157 | CVT-SFA First in Human Trial for Treatment of Superficial Femoral Artery or Pro… | Na | Femoral Artery Stenosis | Completed | 2022-02-17 | 2025-08-27 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05272618 | Coronary Microvascular Dysfunction Assessments in Myocardial Infarction With No… | — | Myocardial Infarction | Recruiting | 2022-02-14 | 2030-12-31 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT05208905 | LIFE-BTK PK Sub-study | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2022-02-10 | 2028-02-22 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT04354077 | Deep Brain Stimulation Effects In Patients With Opioid Use Disorder | Na | Opioid-use Disorder | Recruiting | 2022-02-07 | 2030-01-01 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05198791 | Stratified Medicine of Eplerenone in Acute Myocardial Infarction or Injury and … | Phase2 | Myocardial Infarction, Acute | Recruiting | 2022-02-04 | 2026-07-31 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05252702 | Aveir DR i2i Study | Na | Cardiac Pacemaker, Artificial | Completed | 2022-02-02 | 2026-02-03 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05239208 | Effects of Oral Nutritional Supplementation in Children at Risk of Undernutriti… | Na | Undernutrition | Completed | 2022-01-14 | 2022-12-18 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05242250 | Real-World Evidence Registry to Assess Outcomes of Catheter Ablation for Atrial… | — | Atrial Fibrillation | Terminated | 2022-01-10 | 2023-12-31 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05103527 | Dorsal Root Ganglion Stimulation for the Treatment of Arthritic Knee Pain | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-01-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05433831 | Application of Nutritional Ultrasound in the Diagnosis and Follow-up of Patient… | — | Nutrition Disorders | Unknown | 2022-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05189938 | HbA1c Variation Study | — | Diabetes Mellitus | Completed | 2021-12-20 | 2023-12-30 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT05301218 | CAlcified Lesion Intervention Planning Steered by OCT. | Na | Coronary Artery Calcification | Unknown | 2021-12-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05186779 | Maternal and Newborn Safety Profile of Progestogens in EARLY Pregnancy | — | Early Pregnancy Bleeding | Terminated | 2021-12-15 | 2023-07-14 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT04865978 | Evaluation of the Hemocompatibility of the Direct Oral Anti-Coagulant Apixaban … | Phase2 | Heart Failure | Completed | 2021-12-14 | 2023-11-07 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT05322395 | Pragmatic Randomised Trial of the ESC 0/1 Versus 0/3 Hour Troponin Pathway | Na | Acute Coronary Syndrome | Unknown | 2021-12-10 | 2024-11-10 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT04259411 | MitraClip China PMS | Na | Mitral Regurgitation | Completed | 2021-12-06 | 2025-03-07 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT05168306 | T2 FSL2 Weight Loss | — | Diabetes Mellitus, Type 2 | Terminated | 2021-12-05 | 2023-07-19 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT04997512 | Freestyle Libre and Hospital Admissions in Type 2 Diabetes | Na | Type 2 Diabetes | Unknown | 2021-11-01 | 2025-08-01 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05002088 | Portico Valve-in-Valve Retrospective Registry | — | Aortic Valve Stenosis | Completed | 2021-10-21 | 2023-12-29 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05000840 | Integrating Abbott Point-of-Care Technologies and the Community Scientist Model… | — | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-10-20 | 2025-03-31 | ClinicalTrials.gov |
| NCT05731700 | CVT-ISR First in Human Trial for Coronary In-Stent Restenosis | Na | In-stent Restenosis | Completed | 2021-10-20 | 2025-05-08 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05405335 | Effect of Prone Positioning on the Severity of COVID-19 Pneumonia and Acute Res… | Na | COVID-19 Acute Respiratory Distress Syndrome | Completed | 2021-10-15 | 2022-02-28 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT05731466 | Exercise Right Ventricular Coupling in HFpEF | Na | Heart Failure With Preserved Ejection Fraction | Unknown | 2021-10-13 | 2025-12-31 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT06444386 | ECGi of SyncAV With MultiPoint Pacing | — | Cardiac Resynchronization Therapy | Completed | 2021-09-29 | 2024-04-01 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT04904809 | Perclose Multi-Access Duplex Ultrasound (DUS) Study | Na | Arrhythmia | Completed | 2021-09-01 | 2022-05-27 | ClinicalTrials.gov |
| NCT05040087 | Changing the Natural History of Type 2 Diabetes ("CHANGE" Study) | Na | Type 2 Diabetes | Active_Not_Recruiting | 2021-09-01 | 2027-03-31 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04748965 | Imaging-Guided Vessel Sizing in the Tibial Arteries | — | Peripheral Artery Disease | Completed | 2021-08-16 | 2024-06-09 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04710563 | SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs | — | Peripheral Arterial Disease | Active_Not_Recruiting | 2021-08-11 | 2028-09-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04996277 | A Prospective Evaluation of Clinical Impact of Physiology Versus Optical Cohere… | Na | ST Elevation Myocardial Infarction | Unknown | 2021-07-31 | 2024-03-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04780971 | Use of Physiology to Evaluate Procedural Result After PCI CTO | Na | Percutaneous Coronary Revascularisation | Recruiting | 2021-07-21 | 2026-06-01 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04703855 | Hong Kong and Taiwan HM3 PMS | Na | Advanced Heart Failure | Terminated | 2021-07-14 | 2022-06-30 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04788888 | Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2021-07-13 | 2036-02-28 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT04915937 | Formula Tolerance of Term Infants | Na | Gastro-Intestinal Tolerance | Completed | 2021-07-13 | 2022-11-22 | ClinicalTrials.gov |
| NCT04754217 | Valved Graft PMCF Study | — | Aortic Valve Disease | Recruiting | 2021-07-13 | 2029-09-01 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT05519514 | Bio-Equivalence Study of Budesonide Prolonged-release Tablets 9 Mg In Healthy H… | Phase1 | Healthy Subjects | Completed | 2021-07-12 | 2021-11-15 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04934397 | Term Infants Fed a Partially Hydrolyzed Whey Protein-Based Formula | Na | Gastro-Intestinal Tolerance | Terminated | 2021-07-08 | 2022-02-18 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04942756 | GLYPALCARE STUDY - Multicenter, Randomized Study for Evaluating Continuous Gluc… | Na | Palliative Care | Unknown | 2021-06-30 | 2022-06-30 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT04873817 | Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation | — | Pain | Completed | 2021-06-29 | 2023-03-08 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT05554822 | Head-to-head Comparison of Single Versus Dual Antiplatelet Treatment Strategy A… | Phase3 | Left Atrial Appendage Occlusion | Unknown | 2021-06-14 | 2023-12-31 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04729985 | Diabetes Discharge Transitional CGM Study (DDT-CGM) | Na | Diabetes Mellitus, Type 2 | Active_Not_Recruiting | 2021-06-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05362500 | Comparison of Chemical Peeling Agent With Transamine for Treatment of Melasma | Phase1 | Melasma | Completed | 2021-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT04959552 | FSL2 Post Approval Study for Pediatric and Young Adults Patients | — | Diabete Mellitus | Active_Not_Recruiting | 2021-06-01 | 2026-12-30 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT05659836 | Spinal Cord Stimulation Trial to Permanent Prediction | — | Chronic Pain | Completed | 2021-05-27 | 2023-06-15 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT04818502 | Real World Study of the Tendyne™ Mitral Valve System to Treat Mitral Regurgitat… | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2021-05-04 | 2028-05-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05577637 | Comparitive Study Between Uvb Alone and Uvb With Topical Tacrolimus 0.03% for t… | Phase1 | Vitiligo | Completed | 2021-05-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT05567484 | Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment … | Phase1 | Onychomychosis | Completed | 2021-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04843527 | Evaluation of Flash Continuous Glucose Monitoring to Reduce Hyperglycemia in Pe… | Na | Diabetes Mellitus, Type 2 | Unknown | 2021-04-02 | 2025-06-01 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04809701 | Non-vascular ICD Electrode Configuration Feasibility Study | Na | Ventricular Arrythmia | Completed | 2021-03-22 | 2022-03-24 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04104815 | GI Tolerance and Acceptability of a New Thickener | Na | Gastro-intestinal Tolerance | Withdrawn | 2021-02-05 | 2021-02-05 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | — | Mitral Regurgitation | Recruiting | 2021-02-01 | 2031-03-01 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04431661 | CAOCT: Intra CoronAry Optical Computerized Tomography in out-of Hospital Cardia… | — | Out of Hospital Cardiac Arrest | Terminated | 2021-01-29 | 2023-01-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04784208 | A Study to Determine the Validity and Sensitivity of 'Questionnaire to Screen f… | — | Hypothyroidism | Unknown | 2021-01-18 | 2022-12-31 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04945083 | Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk fo… | Na | Gastrointestinal Tolerance | Completed | 2021-01-13 | 2021-12-09 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04419480 | Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Tr… | Na | Cardiogenic Shock | Recruiting | 2020-12-31 | 2028-12-31 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04464785 | CentriMag Failure-to-Wean Post Approval Study | — | Heart Failure | Completed | 2020-12-30 | 2024-10-25 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04683133 | The FAST OCT Study | Na | Tomography, Optical Coherence | Unknown | 2020-12-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT04489823 | PARADIGM: Amplatzer Valvular Plug for PVL Closure | Na | Paravalvular Aortic Regurgitation | Active_Not_Recruiting | 2020-12-01 | 2026-12-13 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT05175131 | Efficacy and Safety of Mebeverine + Simethicone in Patients With Functional Bow… | Phase3 | Functional Bowel Disorder | Completed | 2020-11-27 | 2021-05-18 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04548128 | Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical S… | — | Advanced Refractory Left Ventricular Heart Failure | Completed | 2020-11-17 | 2022-12-20 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04559945 | The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System | Na | Cardiac Rhythm Disorder | Completed | 2020-11-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04915924 | Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in K… | Na | Advanced Heart Failure | Completed | 2020-10-30 | 2024-06-02 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04650152 | Study to Assess Tricor Therapy Effectiveness in Patients With Metabolic Syndrom… | — | Hypertriglyceridemia | Completed | 2020-10-27 | 2021-11-12 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04604093 | Effect of the FreeStyle Libre 2 Flash Glucose Monitoring System on Hyperglycemi… | — | Diabetes Mellitus | Completed | 2020-10-20 | 2023-03-30 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04942353 | Effects of Home-based Exercise Rehabilitation on Healthcare Utilization in Hear… | Na | Heart Failure | Completed | 2020-10-19 | 2023-04-17 | ClinicalTrials.gov |
| NCT04029454 | Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vacc… | Na | Hepatitis B | Completed | 2020-10-19 | 2023-12-15 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04577976 | FreeStyle Libre 2 Flash Glucose Monitoring System Control Phase Study for Pedia… | — | Diabetes Mellitus | Terminated | 2020-09-23 | 2022-07-14 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04529759 | Healthy Term Infants Fed Milk-Based Infant Formula | Na | Tolerance | Completed | 2020-09-12 | 2021-06-18 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04562714 | Impact of Flash Glucose Monitoring in People With Type 2 Diabetes Using Non-Ins… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-09-08 | 2022-09-06 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04851418 | Pre-hOspital Evaluation of Chest Pain Patients With sUspected Non ST-segment eL… | — | Coronary Artery Disease | Unknown | 2020-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04483089 | An Observational Real-world Study Evaluating Severe Tricuspid Regurgitation Pat… | — | Tricuspid Valve Regurgitation | Active_Not_Recruiting | 2020-08-27 | 2028-01-01 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04345497 | Diabetes-Specific Formula on Long Term Glycemic Control | Na | Diabetes Mellitus, Type 2 | Completed | 2020-08-26 | 2022-12-06 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Na | Critical Limb Ischemia (CLI) | Active_Not_Recruiting | 2020-08-18 | 2027-07-01 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04495738 | Infant Formula and Toddler Drink Feeding Intervention | Na | Respiratory Infections in Children | Terminated | 2020-08-10 | 2021-04-12 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04427124 | The CLI-AMP Registry | — | Critical Limb Ischemia | Unknown | 2020-08-01 | 2023-12-31 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04171960 | Clinical Evaluation of the i-STAT TBI Test | — | Traumatic Brain Injury | Completed | 2020-07-31 | 2023-11-29 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT04479787 | Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT) | Na | Chronic Low-Back Pain | Completed | 2020-07-31 | 2024-02-26 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT05313919 | Coronary Microcirculatory Disease and Inflammation in Patients With Chronic Cor… | — | Coronary Artery Disease | Unknown | 2020-07-24 | 2023-06-30 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04198870 | MitraClip REPAIR MR Study | Na | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-07-21 | 2035-12-01 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04464772 | FreeStyle Libre Continuous Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2020-07-10 | 2020-09-22 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04641416 | Noninvasive Cardiovascular Diagnosis of Patients With Fully Magnetically Levita… | — | End-stage Heart Failure | Unknown | 2020-07-09 | 2025-12-30 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04226547 | Amplatzer Amulet LAAO vs. NOAC | Na | Atrial Fibrillation | Active_Not_Recruiting | 2020-07-07 | 2031-04-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356040 | TactiFlex Paroxysmal Atrial Fibrillation IDE Trial | Na | Paroxysmal Atrial Fibrillation | Completed | 2020-06-29 | 2022-07-01 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04356027 | FUnctional diagnoSIs of corONary Stenosis (FUSION) | — | Coronary Artery Disease | Completed | 2020-06-26 | 2021-10-15 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04900831 | Validation of Beat-to-beat Wavefront Direction Using Omnipolar Mapping | — | Atrial Flutter Typical | Unknown | 2020-06-18 | 2022-08-01 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04282148 | Abbott Next Generation Drug Eluting Stent 48mm Study | Na | Coronary Artery Disease | Completed | 2020-06-17 | 2023-09-17 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04434586 | Contribution of Optical Coherence Tomography in the Endovascular Treatment of F… | Na | Superficial Femoral Artery Stenosis | Recruiting | 2020-06-16 | 2026-06-01 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04460209 | EP Device Registry | — | Cardiac Rhythm Disorder | Completed | 2020-06-12 | 2026-01-31 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04313920 | Study of a Carbohydrate Drink in Adults | Na | Glycemic Response | Completed | 2020-04-07 | 2020-08-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04235062 | NATriuretic Response to Expansion and dIUretics in huMans With Heart Failure | Na | Heart Failure | Completed | 2020-04-01 | 2021-04-26 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04328272 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Phase3 | COVID19 | Unknown | 2020-03-28 | 2020-06-28 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04041908 | Use of a Medical Food in Adults Undergoing Surgery | Na | Compliance, Patient | Terminated | 2020-03-13 | 2020-04-10 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04259437 | Gastrointestinal Tolerance of a Nutritional Supplement in Adult Patients With o… | Na | Gastro-Intestinal Tolerance | Completed | 2020-03-10 | 2021-05-11 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04370691 | JETi Lower Extremity Arterial Thrombosis | — | Arterial Thrombosis | Completed | 2020-03-06 | 2024-10-09 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04249297 | Predictors of Pregnancy Rate in Assisted Reproductive Technology According to A… | — | Infertility | Unknown | 2020-03-03 | 2022-12-01 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04350372 | MitraClip Russia Trial | Na | Functional Mitral Regurgitation | Completed | 2020-02-18 | 2020-10-02 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04253171 | Balloon Lithoplasty for Preparation of Severely Calcified Coronary Lesions | Na | Percutaneous Coronary Intervention | Completed | 2020-01-29 | 2025-11-01 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04180540 | Comparison of Percutaneous Closure to Manual Compression for Hemostasis | Na | Atrial Fibrillation | Completed | 2020-01-22 | 2021-01-13 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04177394 | MitraClip EXPAND G4 Study | — | Mitral Valve Regurgitation | Active_Not_Recruiting | 2020-01-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04180605 | Computational Simulation to Plan for Percutaneous Left Atrial Appendage Closure | Na | Atrial Fibrillation | Unknown | 2020-01-06 | 2022-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04205877 | The U.S. PDA Registry | — | Ductus Arteriosus, Patent | Not_Yet_Recruiting | 2020-01-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04127656 | Infants Fed an Amino Acid-based Formula | Na | Food Allergy | Terminated | 2019-12-16 | 2021-12-16 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04268875 | Morphological Parameters of In-stent RESTenosis Assessed and Identified by OCT | Na | In-stent Restenosis | Completed | 2019-12-11 | 2022-12-06 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04597489 | Fractional FLOw Reserve In Cardiovascular DiseAses | — | Coronary Artery Disease | Completed | 2019-12-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | — | Movement Disorders | Recruiting | 2019-11-26 | 2030-09-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03924661 | SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacemen… | — | Aortic Valve Disease | Active_Not_Recruiting | 2019-10-24 | 2028-10-01 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT03991949 | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula | Na | Infant Development | Completed | 2019-10-04 | 2022-11-16 | ClinicalTrials.gov |
| NCT03786640 | Abbott Brady 3T MRI PMCF | — | Syncope | Completed | 2019-10-04 | 2021-12-18 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04100148 | SyncAV Post-Market Trial | Na | Congestive Heart Failure | Active_Not_Recruiting | 2019-10-03 | 2026-06-30 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04349995 | Amplatzer PFO Occluder Post-marketing Surveillance Study | — | PFO - Patent Foramen Ovale | Completed | 2019-10-01 | 2025-05-28 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04105686 | Growth and Tolerance of Young Infants Fed Infant Formula | Na | Growth and Tolerance | Completed | 2019-09-30 | 2020-12-04 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04011722 | Portico Next Generation Approval Study | Na | Symptomatic Severe Aortic Stenosis | Active_Not_Recruiting | 2019-09-17 | 2033-01-01 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04595305 | Septal Mapping And Resynchronisation Therapy- (SMART) Study | Na | Cardiac Resynchronization Therapy | Completed | 2019-09-16 | 2022-08-23 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT04022954 | HD Mapping of Atrial Fibrillation in Asia Pacific | — | Paroxysmal Atrial Fibrillation | Completed | 2019-09-11 | 2021-08-13 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03940651 | Cardiac and Renal Biomarkers in Arthroplasty Surgery | Phase4 | Renal Injury | Terminated | 2019-09-04 | 2020-09-23 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03363087 | High Density Scar Guided Atrial Fibrillation Mapping | Na | Atrial Fibrillation | Completed | 2019-08-27 | 2023-03-01 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT03882021 | High-Density (HD) Wave Mapping in Subjects With Atrial Fibrillation as a Predic… | Na | Paroxysmal Atrial Fibrillation | Completed | 2019-08-26 | 2022-01-13 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04006236 | Infants Fed Extensively Hydrolyzed Casein-Based Infant Formulas | Na | Infant Development | Completed | 2019-08-05 | 2021-09-20 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT04272411 | SCS Stimulation Clamp to Assess Impact of Stimulation on Glucose Metabolism | Na | Spinal Cord Stimulation (SCS) | Completed | 2019-07-11 | 2020-06-01 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03802942 | Prevention of Hypoglycemia Among Diabetes Patients Admitted to Internal Medicin… | Phase3 | Hypoglycemia | Unknown | 2019-07-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04001452 | 2nd International Survey on Interventional Strategies | — | Coronary Artery Disease | Unknown | 2019-07-01 | 2020-01-31 | ClinicalTrials.gov |
| NCT03989726 | Efficacy of High Density Voltage and Fractionation Map Guided Ablation in Patie… | Na | Atrial Fibrillation | Unknown | 2019-07-01 | 2021-05-31 | ClinicalTrials.gov |
| NCT02997670 | Quartet Lead With Defibrillator Multisite Algorithmic Cardiac Resynchronisation… | Na | Heart Failure, Systolic | Withdrawn | 2019-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03682991 | Reversal of Atrial Substrate to Prevent Atrial | Na | Atrial Fibrillation | Active_Not_Recruiting | 2019-07-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03941314 | A Superiority Trial of the SUPERA Peripheral Stent System in Patients With Femo… | Na | Peripheral Arterial Disease | Completed | 2019-06-25 | 2026-03-19 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03943160 | Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Inte… | — | Peripheral Artery Disease | Completed | 2019-06-11 | 2019-12-11 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03967132 | Growth and Tolerance of Infants Fed Milk-Based Infant Formula | Na | Gastro-Intestinal Tolerance | Completed | 2019-06-08 | 2020-05-29 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03958604 | Burst Neurostimulation for Discogenic Low Back Pain | Na | Discogenic Pain | Completed | 2019-05-28 | 2021-12-31 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03906461 | LSI (Lesion Index) Workflow Observational Study | — | Paroxysmal Atrial Fibrillation | Completed | 2019-05-17 | 2021-04-27 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03951727 | Stella Supera Siberia | Na | Atherosclerosis | Unknown | 2019-05-13 | 2022-05-13 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03677336 | Oral Dydrogesterone (OD) Versus Micronized Vaginal Progesterone (MVP) for Lutea… | Phase4 | Infertility, Female | Completed | 2019-05-01 | 2020-08-24 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03908476 | PROLONG Prospective, Multi-center, Open-label, Post-market Study | Na | Chronic Pain | Completed | 2019-04-16 | 2021-11-15 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT03884231 | A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Condit… | — | Movement Disorders | Completed | 2019-04-10 | 2021-08-20 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03828357 | China (CN)_Magnetic Resonance Imaging (MRI)_Implantable Cardiac Defibrillator (… | — | Tachycardia | Completed | 2019-03-27 | 2020-12-01 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT05307614 | Bioequivalence Study of Moksi® 400mg Tablet and Avelox® 400mg Tablet (Moxifloxa… | Phase1 | Bioequivalence | Completed | 2019-03-27 | 2019-04-27 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03884309 | Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula | Na | Protein Intolerance | Completed | 2019-03-25 | 2020-01-07 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03679832 | A Nutrition-Focused Quality Improvement Program in Hospitalized Malnourished Pa… | — | Malnutrition | Completed | 2019-03-21 | 2019-10-11 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03803995 | Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundl… | Na | Heart Failure | Completed | 2019-03-20 | 2024-04-26 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03690999 | The RAMP Study - Rejuvenation of the Aging Microbiota With Prebiotics | Na | Microbiome | Completed | 2019-03-14 | 2020-12-14 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | — | Chronic Pain | Recruiting | 2019-03-13 | 2029-12-01 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03891823 | Transcatheter Mitral Valve Repair for the Treatment of Mitral Valve Regurgitati… | Na | Ventricular Remodeling, Left | Terminated | 2019-03-08 | 2024-05-15 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03585387 | Cardiac Positioning System in Peripheral Angioplasty Procedure. | — | Peripheral Arterial Disease | Completed | 2019-02-27 | 2020-06-09 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03724812 | FlexNav EU CE Mark Study | Na | Symptomatic Severe Aortic Stenosis | Completed | 2019-02-26 | 2021-02-10 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03815175 | XIENCE 28 USA Study | Na | Bleeding Disorder | Completed | 2019-02-25 | 2021-02-04 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03705312 | MitraClip for the Treatment of Moderate Functional Mitral Regurgitation: EVOLVE… | Na | Mitral Regurgitation | Unknown | 2019-02-22 | 2022-01-01 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03820050 | FreeStyle LIbre Flash Glucose Monitoring System Pediatric Accuracy Study | — | Diabetes Mellitus | Completed | 2019-01-29 | 2019-06-14 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03825419 | Detection of Muscle Loss in Acute Stroke Patients Who Need Enteral Nutrition (M… | — | Acute Ischemic Stroke | Completed | 2019-01-23 | 2021-11-30 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT03733392 | Advisor HD Grid Observational Study | — | Persistent Atrial Fibrillation | Completed | 2019-01-11 | 2021-05-27 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT05746416 | Xience Registry In Complex Lesion of Acute Coronary Syndrome Patients witH Tica… | — | Coronary Artery Disease | Completed | 2019-01-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03447834 | EUROpean Intracoronary Cooling Evaluation in Patients With ST-elevation Myocard… | Na | Acute Myocardial Infarction | Unknown | 2019-01-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT00613418 | Comparative Study Of Safety And Efficacy Of The SUPERA® Nitinol Stent - Iliac A… | Na | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | Withdrawn | 2019-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781258 | Anti-thrombotic Monotherapy in HeartMate 3 Left Ventricular Assist System (LVAS) | Na | Heart Failure | Unknown | 2018-11-23 | 2021-12-31 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03701867 | Muscle Energy Metabolism and Metabolic Flexibility in Older Men and Women | Na | Energy Metabolism | Completed | 2018-11-14 | 2019-07-22 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03803969 | ConfirmRxTM: Posture and Activity | Na | Syncope | Completed | 2018-10-30 | 2020-07-30 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03785418 | Lifestyle Modification for the Treatment of Symptomatic Atrial Fibrillation (LI… | Na | Atrial Fibrillation | Unknown | 2018-10-29 | 2020-07-01 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03752866 | CONFIDENCE Registry to Assess Safety and Performance of Portico System to Treat… | Na | Symptomatic Degenerative Aortic Stenosis | Completed | 2018-10-25 | 2022-07-28 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03561051 | The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study | — | Chest Pain | Active_Not_Recruiting | 2018-10-16 | 2025-01-01 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03539458 | Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcific… | Na | Mitral Regurgitation | Completed | 2018-10-10 | 2024-06-18 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03567096 | LV Only MPP With SyncAV | Na | Heart Failure | Completed | 2018-10-09 | 2023-09-30 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03165526 | The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption… | — | Post-Infarction Ventricular Septal Defect | Completed | 2018-10-01 | 2021-11-29 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03650556 | Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCat… | Na | Persistent Atrial Fibrillation | Completed | 2018-09-28 | 2021-01-11 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03690765 | Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone … | — | Endometriosis | Completed | 2018-09-27 | 2020-05-29 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT03628196 | A Nutrition-Focused QIP in Outpatient Clinics | — | Malnutrition | Completed | 2018-09-26 | 2020-03-18 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT04475380 | Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xien… | — | Acute Coronary Syndrome | Completed | 2018-09-21 | 2025-12-31 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03628183 | Tolerance of Infants Fed a Hydrolysate Formula | Na | Gastrointestinal Tolerance | Completed | 2018-08-28 | 2018-11-23 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03473561 | Study to Evaluate the Efficacy and Safety of Racecadotril in Children Aged 3 to… | Phase3 | Diarrhea, Infantile | Completed | 2018-08-25 | 2020-01-08 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT03704220 | Anti-thrombotic Monotherapy With the HeartMate 3 LVAS | Na | Heart Failure | Unknown | 2018-08-16 | 2021-12-01 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT04397224 | Reduction or Extension of COnduction Time With Ventricular Electromechanical Re… | — | Heart Failure | Unknown | 2018-07-20 | 2024-07-20 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03564860 | HBP Device EGM Data Collection | — | Sick Sinus Syndrome | Completed | 2018-07-17 | 2020-09-30 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03630302 | Intraoperative Investigation of a Directional Lead and Local Field Potentials f… | — | Parkinson | Completed | 2018-07-12 | 2020-01-31 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03433274 | Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Tr… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-06-15 | 2028-06-01 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03459001 | Evaluation of a High Calorie, High Protein Tube Feeding Product in an Adult Pop… | — | Malnutrition | Completed | 2018-06-08 | 2019-02-07 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03632057 | Shock Efficacy Study Comparing Fixed Tilt and Fixed Pulse Width in a General Im… | Na | Ventricular Arrythmia | Completed | 2018-06-06 | 2025-04-18 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03720639 | Confirm Rx™ Versus Reveal LINQ™ - Which is More Reliable in Data Transmission? … | Na | Cardiac Arrythmias | Completed | 2018-05-18 | 2020-03-09 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03507777 | ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI) | Na | Coronary Artery Disease | Completed | 2018-05-17 | 2023-02-28 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03508154 | Evaluation of Carbohydrates - Glycemic Index | Na | Glycemic Index | Completed | 2018-05-07 | 2018-05-22 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03458013 | Psychosocial Outcomes in Hand Therapy | Na | Hand Injuries | Completed | 2018-05-01 | 2020-01-22 | ClinicalTrials.gov |
| NCT03503851 | Noninferiority Trial of MitraClip Implantation Strategies: 1 Clip vs. 2 Clips i… | Na | Mitral Regurgitation Functional | Withdrawn | 2018-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03502811 | The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices | — | Mitral Valve Regurgitation | Completed | 2018-04-26 | 2020-12-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03505801 | Confirm Rx Insertable Cardiac Monitor SMART Registry | — | Cardiac Arrhythmias | Active_Not_Recruiting | 2018-04-24 | 2026-03-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03548506 | Subthalamic Steering for Therapy Optimization in Parkinson's Disease | Na | Parkinson Disease | Completed | 2018-04-19 | 2023-12-31 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03502174 | FreeStyle Libre Glucose Monitoring System in Pediatric Populations | — | Diabetes Mellitus | Completed | 2018-04-05 | 2018-07-03 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03744000 | Deferred Stenting in Patients With Anterior Wall STEMI | Na | Acute Myocardial Infarction With ST Elevation | Active_Not_Recruiting | 2018-04-03 | 2025-11-30 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03500692 | MitraClip NT System Post-marketing Surveillance Study - Japan | — | Mitral Regurgitation | Completed | 2018-04-02 | 2022-03-23 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03463512 | Controlled Study to Evaluate the Efficacy and Safety of Racecadotril in Infants… | Phase3 | Diarrhea | Completed | 2018-03-29 | 2018-09-10 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03387813 | Hemodynamic-GUIDEd Management of Heart Failure | Na | Heart Failure | Completed | 2018-03-15 | 2023-05-17 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03271762 | Multicentre Study of MITRACLIP® Transcatheter Mitral Valve Repair in Patients W… | Na | Mitral Regurgitation | Active_Not_Recruiting | 2018-03-02 | 2028-01-01 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03448367 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study for Pediatr… | — | Diabetes Mellitus | Terminated | 2018-02-27 | 2020-10-13 | ClinicalTrials.gov |
| NCT03448380 | FreeStyle Libre Flash Glucose Monitoring System Post Approval Study | — | Diabetes Mellitus | Completed | 2018-02-27 | 2021-03-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03355742 | XIENCE 28 Global Study | Na | Bleeding Disorder | Completed | 2018-02-09 | 2020-04-30 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03309332 | AMPLATZER PFO Occluder Post Approval Study | Na | Stroke | Active_Not_Recruiting | 2018-01-31 | 2030-02-05 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03597113 | Evaluation of Infants Fed an Extensively Hydrolyzed Hypo Allergenic Infant Form… | — | Gastrointestinal Tolerance | Completed | 2018-01-31 | 2020-03-27 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03415152 | A Prospective Observational Program Using Digital Technology Tools to Enhance P… | — | History of Myocardial Infarction | Completed | 2018-01-24 | 2019-07-01 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03667196 | Evaluation of Effectiveness and Safety of Antegrade and Retrograde Approach of … | — | Chronic Total Occlusion of Coronary Artery | Recruiting | 2018-01-11 | 2032-12-31 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03549143 | Multicenter Observational Prospective Study to Describe Irritable Bowel Syndrom… | — | Irritable Bowel Syndrome | Completed | 2017-12-25 | 2019-04-19 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03354663 | TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2017-12-11 | 2019-10-30 | ClinicalTrials.gov |
| NCT03369899 | FreeStyle Libre Flash Glucose Monitoring System in Pediatric Populations | — | Diabete Mellitus | Completed | 2017-12-11 | 2018-05-23 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT04682483 | Cardiogenic Shock Working Group Registry | — | Cardiogenic Shock | Recruiting | 2017-12-04 | 2026-06-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT03315884 | Pilot Randomized Clinical Study of the Iliac Arteries and Common Femoral Artery… | Na | Atherosclerosis of the Peripheral Arteries | Unknown | 2017-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01643746 | Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusiv… | Na | Femoropopliteal Stenosis | Withdrawn | 2017-12-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03338374 | Cardiac Resynchronisation Therapy Versus Rate-responsive Pacing in Heart Failur… | Na | Diastolic Heart Failure | Completed | 2017-11-27 | 2022-05-30 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT03214029 | COmparisoN of High-sensitivity Cardiac TRoponin I and T ASsays Trial | — | Acute Myocardial Infarction | Active_Not_Recruiting | 2017-11-06 | 2025-12-31 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT02924285 | Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contra… | Phase3 | Heart Diseases | Completed | 2017-11-01 | 2021-03-04 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03350256 | BurstDR™ micrOdosing stimuLation in De-novo Patients | Na | Pain, Intractable | Completed | 2017-10-30 | 2019-07-02 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03153397 | Effect of Prebiotic Fiber- Enriched (scFOS) Enteral Feeding on the Microbiome i… | Na | Enteral Nutrition | Completed | 2017-10-23 | 2021-05-31 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03489603 | Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation… | — | NSTEMI - Non-ST Segment Elevation MI | Completed | 2017-10-11 | 2019-06-15 | ClinicalTrials.gov |
| NCT03276884 | Growth and Tolerance of Young Infants | Na | Growth | Completed | 2017-10-11 | 2018-11-08 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03451617 | Alpine vs. Xpedition: Evaluation of Stent Delivery System | Na | Percutaneous Coronary Intervention | Unknown | 2017-10-05 | 2020-10-05 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03277378 | Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therap… | Na | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | Completed | 2017-09-22 | 2018-10-12 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03293706 | Evaluation of Carbohydrates Part 2 | Na | Gastro-Intestinal Tolerance | Completed | 2017-09-21 | 2017-11-15 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03213340 | Effects of Phytonutrients Upon Muscle Perfusion in Response to Feeding | Na | Biological Aging | Completed | 2017-09-14 | 2019-10-02 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03450772 | Equivalence Study to Compare Two Strengths of Creon in China | Phase3 | Pancreatic Insufficiency | Unknown | 2017-08-31 | 2022-04-30 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03240952 | The Nutritional Health for the Elderly Reference Centre Study (NHERC Study) | — | Malnutrition | Completed | 2017-08-30 | 2018-07-26 | ClinicalTrials.gov |
| NCT03245047 | The Nutritional Health for the Elderly Reference Centre Study (The NHERC Study) | Na | Malnutrition | Completed | 2017-08-30 | 2020-03-10 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03244683 | A Study of the Efficacy of ONS to Reduce Postoperative Complications Associated… | Na | Pancreatic Cancer | Terminated | 2017-08-28 | 2018-08-01 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03247829 | Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Dev… | — | Heart Failure | Completed | 2017-08-24 | 2020-06-30 | ClinicalTrials.gov |
| NCT03811938 | Ablation of Low Voltage Regions in Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Unknown | 2017-08-24 | 2020-06-01 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03257501 | FreeStyle Libre Flash Accuracy Study | — | Diabetes Mellitus | Completed | 2017-08-22 | 2018-01-08 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03455374 | Diamondback in Peripheral Vascular Disease | Na | Peripheral Vascular Diseases | Terminated | 2017-08-08 | 2019-05-13 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT03227757 | TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With… | Na | Tricuspid Valve Insufficiency | Completed | 2017-08-01 | 2024-05-30 | ClinicalTrials.gov |
| NCT02943616 | ABSORB Post-Approval Clinical Study | Na | Ischemic Heart Disease | Withdrawn | 2017-08-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT02814578 | Assessment of Coronary Artery Lesion Using Optical Coherence Tomography Versus … | Na | Coronary Artery Disease | Terminated | 2017-07-31 | 2017-07-31 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03218787 | XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HB… | Na | Coronary Artery Lesions | Completed | 2017-07-19 | 2020-09-04 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03242122 | Evaluation of Carbohydrates | Na | Glycemic Index | Completed | 2017-07-17 | 2017-08-18 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03171311 | The OCTOBER Trial - European Trial on Optical Coherence Tomography Optimized Bi… | Na | Ischaemic Heart Disease | Active_Not_Recruiting | 2017-07-05 | 2029-05-01 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03055858 | AMPLATZER Duct Occluder II Additional Sizes | Na | Patent Ductus Arteriosus | Completed | 2017-06-05 | 2022-04-05 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03001141 | Study Protocol/ Registry of MultiPoint™ Pacing in Brazil | — | Heart Failure, Unspecified | Terminated | 2017-05-18 | 2019-02-08 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03084991 | OPTical Coherence Tomography IMAging in Patients With Acute myocardiaL Infarcti… | — | Acute Myocardial Infarction | Unknown | 2017-05-17 | 2022-12-01 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03159546 | FreeStyle Libre Flash Glucose Monitoring System Accuracy | — | Diabete Mellitus | Completed | 2017-05-13 | 2017-08-24 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT03073447 | WAMIF : Young Women Presenting Acute Myocardial Infarction in France | Na | Acute Myocardial Infarction | Completed | 2017-05-04 | 2020-10-06 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT02830152 | Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Pa… | Na | Atrial Fibrillation | Active_Not_Recruiting | 2017-05-03 | 2028-12-01 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03175315 | Evaluation of a Treatment and Education Program for Diabetic Patients Who Use F… | Na | Diabetes Mellitus | Completed | 2017-05-02 | 2018-03-09 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03141892 | FreeStyle Libre Flash Glucose Monitoring System Accuracy Study | — | Diabetes Mellitus | Completed | 2017-04-13 | 2017-05-30 | ClinicalTrials.gov |
| NCT03041233 | ABLATOR Brazil - Ablation Observational Study (Registry) | — | Atrial Fibrillation | Completed | 2017-04-13 | 2020-04-27 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT02963259 | IPG Replacement Study (PREFERENCE-H) | — | Parkinson Disease | Completed | 2017-03-29 | 2020-01-31 | ClinicalTrials.gov |
| NCT03056573 | Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alte… | Na | Aortic Valve Stenosis | Completed | 2017-03-29 | 2019-07-05 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03108456 | Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbit… | Na | Coronary Artery Disease | Unknown | 2017-03-27 | 2025-06-12 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03061929 | Human Milk Composition in Indian Mothers | — | Breast Feeding | Completed | 2017-03-24 | 2019-06-30 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03016169 | Trifecta™ GT Post Market Clinical Follow-up | Na | Aortic Valve Disease | Completed | 2017-03-09 | 2023-08-31 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03082261 | Multi-center Prospective Study Determining the Sustainability of Pain Relief an… | Na | Chronic Pain | Completed | 2017-03-03 | 2020-08-26 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03048890 | VascTrac Peripheral Arterial Disease (PAD) Study | — | Peripheral Artery Disease | Unknown | 2017-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03055910 | Fractional Flow Reserve Fax Registry | — | Coronary Artery Disease | Unknown | 2017-03-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT03082599 | Symfony Toric Intraocular Lens Visual Outcomes | Na | Cataract Bilateral | Completed | 2017-02-17 | 2018-04-03 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT04230889 | Evaluation of Glucose Control in Patients With Diabetes | Na | Glycemic Control | Completed | 2017-02-06 | 2018-02-15 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03052803 | Comparison of Devices Evaluating Fractional Flow Reserve in Coronary Arteries | — | Coronary Artery Disease | Completed | 2017-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03078374 | MAGENTUM 1 HeartMate 3 LVAS: A Single Center Prospective Controlled Study (MAGE… | Na | Heart Failure | Unknown | 2017-01-11 | 2022-10-01 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03117426 | A Randomised Evaluation of Visual Function After Bilateral Implantation of Two … | Na | Cataract | Completed | 2017-01-01 | 2017-10-30 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03036956 | The Prevalence of Sub Clinical Hypothyroidism During Early Pregnancy in Pakistan | — | Subclinical Hypothyroidism | Completed | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02471729 | Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance… | Phase1 | Chronic Heart Failure | Unknown | 2017-01-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT03409731 | Absorb GT1 Japan PMS | Na | Ischemic Heart Disease | Completed | 2016-12-13 | 2023-02-06 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02964208 | AMPLATZER™ LAA Occluder Post Approval Study (PAS) | — | Atrial Fibrillation | Completed | 2016-12-08 | 2022-08-10 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02931435 | Radiofrequency For Chronic Knee Pain Post-Arthroplasty | Na | Chronic Knee Pain | Completed | 2016-12-01 | 2018-11-30 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT03020290 | Long Superficial Femoral Artery Stenting With SuperA Interwoven Nitinol Stents | — | Atherosclerosis Obliterans | Completed | 2016-12-01 | 2018-04-10 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02943954 | FLOW Evaluation to Guide Revascularization in Multi-vessel ST-elevation Myocard… | Na | Acute ST Segment Elevation Myocardial Infarction | Unknown | 2016-12-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02903940 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-12-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698540 | A Study of an Oral Nutritional Supplement in a Malnourished Population With GI … | — | Malnutrition | Completed | 2016-11-28 | 2018-05-01 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT02954237 | AMPLATZER™ Cardiac Plug Observational Post-Approval Study | — | Non-valvular Atrial Fibrillation (NVAF) | Completed | 2016-11-14 | 2021-01-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT03012568 | Clinical Study to Confirm MRI Safety and Effectiveness Using St. Jude Medical (… | — | Bradycardia | Completed | 2016-11-10 | 2018-03-29 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02858245 | A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgit… | — | Mitral Regurgitation | Terminated | 2016-11-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02844127 | Effect of Right Ventricular Lead Position on Defibrillation Threshold | Na | Ventricular Tachycardia | Withdrawn | 2016-11-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT02836652 | Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients With… | Phase4 | Heart Failure | Completed | 2016-11-01 | 2019-07-18 | ClinicalTrials.gov |
| NCT02986074 | CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming S… | Na | Chronic Pain | Completed | 2016-11-01 | 2019-08-19 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT03237169 | Performance of a New REsting Pressure Index During Invasive Angiography Compare… | — | Fractional Flow Reserve, Myocardial | Unknown | 2016-10-28 | 2018-09-01 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02738840 | A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditiona… | Na | Chronic Pain | Completed | 2016-10-21 | 2020-12-02 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02935088 | PRESSUREwire Study | — | Coronary Artery Disease | Completed | 2016-10-12 | 2019-03-22 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02877693 | A Post-market Clinical Evaluation of St. Jude Medical™ MR Conditional ICD Syste… | Na | ICD | Completed | 2016-10-10 | 2020-03-23 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02360722 | Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly | Phase4 | Malnutrition | Withdrawn | 2016-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT04756180 | An Efficacy and Safety Study of Omega-3-acid Ethyl Ester in Chinese Subjects Wi… | Phase3 | Hypertriglyceridemia | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02830360 | Antiarrhythmics or Ablation for Ventricular Tachycardia 2 | Phase4 | Ventricular Tachycardia (VT) | Completed | 2016-10-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02923960 | Effect of Nutritional Products in Subjects With Type 2 Diabetes | Na | Diabetes | Completed | 2016-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02950831 | Objective Assessment of Activity and Sleep Quality In Burst Spinal Cord Stimula… | Na | Chronic Pain | Completed | 2016-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02913638 | A Post Breastfeeding Follow-Up Study | — | Breast Feeding | Completed | 2016-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02910362 | Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Ver… | Na | Cataract Surgery | Completed | 2016-09-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02806765 | Effect of Dietary Supplementation on Dynamic Stability | Na | Aging | Withdrawn | 2016-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03098368 | Rotigotine Effect on Nocturnal Hypokinesia Compares to Placebo Control: A Quant… | Phase4 | Nocturnal Hypokinesia | Unknown | 2016-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02879448 | AMPLATZER™ Amulet™ LAA Occluder Trial | Na | Stroke | Completed | 2016-08-24 | 2024-05-24 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02800863 | TARGET Post-Approval Study | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2016-08-23 | 2021-09-23 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02862119 | Ffr-gUidance for compLete Non-cuLprit REVASCularization | Na | Coronary Artery Disease | Completed | 2016-08-08 | 2023-07-17 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02892955 | MOMENTUM 3 Continued Access Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2016-08-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02750787 | Use of a Peptide-based Formula in an Adult Population | Na | Malabsorption | Completed | 2016-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02776007 | Patients Perceptions of Using the "Libre" System Compared With Conventional SMB… | Na | Type 1 Diabetes | Completed | 2016-07-01 | 2020-04-30 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02832622 | MultiPoint Pacing™ Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2019-07-15 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02896361 | Burst Optimized Stimulation Study | Na | Chronic Pain | Completed | 2016-07-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02954341 | CardioMEMS HF System OUS Post Market Study | — | Heart Failure | Completed | 2016-07-01 | 2023-12-08 | ClinicalTrials.gov |
| NCT02173860 | Strategies for Revascularization in Patients Undergoing Heart Valve Surgery Wit… | Na | Coronary Artery Disease | Unknown | 2016-07-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02825134 | Comparison of TAVR With SAVR in Younger Low Surgical Risk Patients With Severe … | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-06-30 | 2029-06-01 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02821117 | FreeStyle Libre Glucose Monitoring System Paediatric Study | Na | Diabetes Mellitus | Completed | 2016-06-30 | 2017-02-22 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02728739 | Incidence of Significant Mitral Regurgitation in Acute Heart Failure Patients | Na | Acute Heart Failure | Completed | 2016-06-06 | 2018-02-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02782598 | The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2016-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02814214 | Device-based QRS Evaluation | — | Heart Failure | Completed | 2016-06-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02807948 | SJM MRI Diagnostic Imaging Registry (IDE) | Na | Cardiac Arrhythmia | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02799043 | Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With F… | Na | Persistent Atrial Fibrillation | Completed | 2016-06-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02928198 | Bifurcation ABSORB OCT Trial | Na | Myocardial Ischemia | Unknown | 2016-06-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT02787291 | A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse … | Na | Implantable Defibrillator User | Completed | 2016-05-01 | 2018-04-11 | ClinicalTrials.gov |
| NCT02706574 | Brain Injury Assessment Study at Hennepin County Medical Center | — | Traumatic Brain Injury | Unknown | 2016-05-01 | 2022-07-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03047603 | Evaluation of Diagnostic Efficiency of PIVKA-II and Other Tumor Markers in HCC | — | Hepatocellular Carcinoma | Completed | 2016-05-01 | 2019-03-20 | ClinicalTrials.gov |
| NCT03167424 | Restenosis Intrastent: Treatment of Bioresorbable Vascular Scaffolds Restenosis | — | Coronary In-stnent Restenosis | Unknown | 2016-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02693691 | CardioMEMS European Monitoring Study for Heart Failure | Na | Heart Failure | Completed | 2016-05-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02676466 | The ENRGISE (ENabling Reduction of Low-Grade Inflammation in SEniors) Pilot Stu… | Phase2 | Inflammation | Completed | 2016-04-26 | 2018-06-22 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02732158 | Novel Laboratory Methods in Nutrition Studies | Na | Healthy | Completed | 2016-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02746016 | Effect of Formula on Infant Behavior | Na | Gastrointestinal Tolerance | Completed | 2016-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02649842 | Post-Approval Study of the TECNIS® Toric Extended Cylinder Range Intraocular Le… | Na | Cataract | Completed | 2016-03-21 | 2019-01-28 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02698150 | Remote Monitoring of Patients With Functional Mitral Regurgitation Undergoing M… | — | Mitral Regurgitation | Unknown | 2016-03-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02722577 | EGM Analysis in Idiopathic Outflow Tract Ventricular Arrhythmia | — | Ventricular Outflow Tract Tachycardia | Completed | 2016-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02675751 | Prospective S&E Study of Wavefront-guided PRK for Myopia With iDesign Advanced … | Na | Stable Myopic Refractive Error, With or Without Astigmatism | Completed | 2016-02-03 | 2018-07-27 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02703454 | FIRM Ablation Versus Pulmonary Vein Isolation for the Treatment of Paroxysmal A… | Na | Paroxysmal Atrial Fibrillation | Terminated | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02699060 | Experimental Study to Determine the Effects of Human Refluxate on Macrophage Ph… | Na | Gastroesophageal Reflux Disease (GERD) | Completed | 2016-02-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02476201 | Quartet Lead and Resynchronization Therapy Options III (QUARTO_III) | Na | Heart Failure | Completed | 2016-02-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT02758002 | Inhibition of Atrial Fibrillation by Elimination of Transitional Mechanisms | Na | Atrial Fibrillation | Withdrawn | 2016-01-28 | 2018-12-01 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT03058510 | Feasibility of Orbital Atherectomy System in Calcified Bifurcation Lesion | — | Coronary Artery Disease | Completed | 2016-01-17 | 2017-10-13 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02168829 | Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atr… | Phase4 | Atrial Fibrillation | Completed | 2016-01-01 | 2025-08-14 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02613780 | Refractive Treatment of Early Keratoconus | Phase3 | Keratoconus | Unknown | 2016-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02665455 | FreeStyle Libre in Pregnancy Study | Na | Diabetes Mellitus | Completed | 2016-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02779621 | The Potential for HPV Self-testing to Promote Participation in Cervical Screeni… | Na | Cervix Diseases | Withdrawn | 2016-01-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02847572 | Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Mul… | Na | Cataract | Completed | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03069066 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment With Scoring … | Phase4 | Coronary In-stent Restenosis | Unknown | 2016-01-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02634398 | A Post Market Study on DRG Stimulation in FBSS (SYMPATHY) | — | Failed Back Surgery Syndrome | Withdrawn | 2015-12-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02648230 | PrEssure wiRe Compared to Microcatheter-based Sensing Technology For the Evalua… | Na | Ischemia | Completed | 2015-12-01 | 2016-12-08 | ClinicalTrials.gov |
| NCT02377947 | A Retrospective, Open-label, Uncontrolled Cohort Study to Assess the Effectiven… | — | Hepatic Encephalopathy | Completed | 2015-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02613858 | Minimal HePatic Encephalopathy Among CiRrhotics. A Cross SEctional, Clinico-Epi… | — | Hepatic Encephalopathy | Completed | 2015-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT02548455 | Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE)… | Na | Heart Failure | Completed | 2015-10-27 | 2017-03-21 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT03085316 | Laryngeal Pacing Study | Na | Bilateral Vocal Fold Paralysis (BVFP) | Terminated | 2015-10-26 | 2023-11-07 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02566083 | Post-Approval Study of the Tecnis® Toric IOL | Na | Cataract | Completed | 2015-10-21 | 2019-05-23 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02789904 | Evaluation of hsTnI in the Management of Patients With Chest Pain in the Emerge… | — | Chest Pain | Completed | 2015-10-05 | 2017-11-01 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02587637 | Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back … | Na | Chronic Pain | Completed | 2015-10-01 | 2018-01-30 | ClinicalTrials.gov |
| NCT02596321 | A Study Investigating the Immunologic Effects and Safety of 60-day Treatment of… | Phase3 | Allergy | Completed | 2015-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT02520310 | AVJ-514 Japan Trial | Na | Mitral Stenosis With Insufficiency | Completed | 2015-09-07 | 2021-05-31 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT06306066 | Coronary Thermo-dilution Derived Flow-indices in Chronic Coronary Syndrome | — | Coronary Artery Disease | Completed | 2015-09-02 | 2022-12-28 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02584595 | Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients … | — | Monomorphic Ventricular Tachycardia | Withdrawn | 2015-09-01 | 2022-02-01 | ClinicalTrials.gov |
| NCT02561299 | Orbital Vessel PreparaTIon to MaximIZe Dcb Efficacy in Calcified Below the Knee… | Na | PAD | Completed | 2015-09-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT02553408 | Patients and Care Providers Perspectives and Experience With Decision Aid Tool … | Na | Type 2 Diabetes | Completed | 2015-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02592889 | (MitraClip in Non-Responders to Cardiac Resynchronization Therapy) | Phase4 | MITRAL REGURGITATION | Unknown | 2015-09-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02470312 | MediGuide Registry | — | Heart Failure | Terminated | 2015-08-18 | 2018-02-28 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02863159 | A Clinical Assessment of the Full Range of Functional Vision With Three Tecnis … | Na | Cataract | Unknown | 2015-08-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02468778 | SHIELD II Clinical Investigation | Na | Coronary Artery Disease | Terminated | 2015-08-01 | 2021-05-17 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02656537 | EnSite™ HD Grid Catheter AF/AT Mapping Study | Na | Non-paroxysmal Atrial Fibrillation | Completed | 2015-08-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02845804 | Effect and Efficacy of Xpedition™/Alpine™, Everolimus-eluting Stent for Coronar… | — | Coronary Artery Disease | Unknown | 2015-07-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02492386 | Bioabsorbable Everolimus-Eluting Stents for Internal Pudendal Artery-Related Ar… | Phase2 | Impotence, Arteriogenic | Unknown | 2015-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02491437 | A Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone … | Phase3 | Female Infertility | Completed | 2015-07-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02489331 | Post Marketing Surveillance of Safety and Efficacy for Cholib in Korean Patient… | — | Dyslipidemias | Completed | 2015-07-01 | 2020-11-10 | ClinicalTrials.gov |
| NCT02571218 | AF Substrate Mapping and Guided Ablation | Na | Persistent Atrial Fibrillation | Completed | 2015-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02577887 | Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II | — | Standard Bradycardia Pacing Indication | Completed | 2015-07-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT02260154 | Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointest… | — | Post-cholecystectomy Gastrointestinal Spasms | Completed | 2015-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02097420 | HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotat… | Na | Mitral Valve Disease | Completed | 2015-05-07 | 2023-07-01 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02471586 | OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiogra… | Na | Coronary Artery Disease | Completed | 2015-05-01 | 2017-04-25 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02475460 | HeartMate 3™ LIS Study | Na | Heart Failure | Completed | 2015-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02407249 | Topera C-FIRM Registry | — | Atrial Fibrillation | Completed | 2015-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02401217 | Tolerance of Healthy Infants Fed Infant Formulas | Na | Gastrointestinal Tolerance | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02434315 | FreeStyle Libre Pro Use in Primary & Secondary Care | Na | Diabetes Mellitus | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02381418 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2015-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02339545 | Coronary Flow Reserve Following Orbital Atherectomy | — | Coronary Artery Disease | Completed | 2015-02-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02310100 | TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post A… | Na | Paroxysmal Atrial Fibrillation | Completed | 2015-01-21 | 2021-09-17 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02353351 | ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study | — | Atrial Septal Defect Secundum | Terminated | 2015-01-19 | 2017-02-24 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02337699 | Dorsal Root Ganglion Stimulation as Treatment for Post-surgical Groin Pain | — | Post Surgical Groin Pain | Terminated | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02322138 | Gastrointestinal Tolerance of Infant Formula | Na | Gastrointestinal Tolerance | Completed | 2015-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02336945 | Glucose Variability Pilot Study for the Abbott Sensor Based Glucose Monitoring … | — | Type 2 Diabetes Mellitus | Completed | 2015-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02279888 | CardioMEMS HF System Post Approval Study | — | Heart Failure | Completed | 2015-01-01 | 2019-10-11 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02367716 | Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese … | — | Chronic Heart Failure | Completed | 2014-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02307760 | Evaluation of Human Milk Fortifiers in Preterm Infants | Na | Infant Growth | Completed | 2014-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02421549 | Remote Interrogation in Rural Emergency Departments | Phase4 | Heart Disease | Withdrawn | 2014-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02344173 | ABLATOR Ablation Observational Registry | — | Atrial Fibrillation | Completed | 2014-11-01 | 2017-08-18 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02130765 | Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for… | Na | Monomorphic Ventricular Tachycardia | Terminated | 2014-11-01 | 2016-07-25 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02321514 | Expanded Clinical Study of the Tendyne Mitral Valve System | Na | Mitral Valve Regurgitation | Completed | 2014-11-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01989299 | Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients… | — | Heart Failure With Preserved Ejection Fraction (HFpEF) | Completed | 2014-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02305342 | Sensitivity of Antibiotics for Urinary Tract Infections Patients Attending Fami… | — | Urinary Tract Infections (UTIs) | Completed | 2014-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02283411 | Effectiveness and Safety Study of the Abbott Sensor Based Glucose Monitoring Sy… | Na | Diabetes Mellitus, Type 1 | Completed | 2014-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT01722942 | Amiodarone Against ICD Therapy in Chagas Cardiomyopathy for Primary Prevention … | Na | Chagas Cardiomyopathy | Unknown | 2014-10-06 | 2022-07-31 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02150473 | The Effect of Adalimumab Plus Methotrexate (MTX) Versus Placebo Plus MTX on Car… | Phase3 | Rheumatoid Arthritis | Terminated | 2014-10-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02298556 | An Observational Study to Describe the Effectiveness of Angiotensin Converting … | — | Hypertension | Completed | 2014-10-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02279979 | Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial | Na | Cardiogenic Shock | Terminated | 2014-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02245360 | Study Immunology and Safety of 60-day Treatment of SQ Grass SLIT (Sublingual Im… | Phase3 | Seasonal Allergic Rhinitis | Completed | 2014-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02989090 | Electronic Patient Notification of Remote ICD Data: Impact of Patient Engagemen… | Na | Implantable Cardioverter-Defibrillator | Completed | 2014-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT02224755 | MOMENTUM 3 IDE Clinical Study Protocol | Na | Advanced Refractory Left Ventricular Heart Failure | Completed | 2014-09-02 | 2019-03-26 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02158403 | PREVENtion of HeartMate II Pump Thrombosis | Na | HeartMate II Pump Thrombosis | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02203721 | Clinical Investigation of a New Intraocular Lens | Na | Cataract | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01911078 | Renal Sympathetic Denervation in Metabolic Syndrome (Metabolic Syndrome Study) | Na | Metabolic Syndrome | Completed | 2014-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02250469 | A Randomised Pilot Study to Assess Differences in Stimulation Induced Paresthes… | Na | Chronic Pain | Terminated | 2014-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02262286 | MIND (Management of Traumatic Brain Injury Diagnosis) | — | Brain Injury | Completed | 2014-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02232698 | An Evaluation of Novel Glucose Sensing Technology on Hypoglycaemia in Type 1 Di… | Na | Type 1 Diabetes Mellitus | Completed | 2014-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02213120 | To Study the Characteristics of Different Types of Vertigo in Patients Attendin… | — | Vertigo | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02060630 | Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Isch… | Na | Critical Limb Ischemia | Completed | 2014-08-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02195843 | Quadripolar Leads for the Management of Heart Failure Patients in the Middle Ea… | Phase4 | Heart Failure | Unknown | 2014-08-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT01614717 | Triple Chamber Pacing in Hypertrophic Obstructive Cardiomyopathy (HOCM) Patient… | Na | Hypertrophic Cardiomyopathy With Obstruction | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02513732 | XIENCE Xpedition Everolimus-Eluting Coronary Stent Japan Post Marketing Surveil… | — | Ischemic Heart Disease | Completed | 2014-07-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02193971 | Harmonizing Optimal Strategy for Treatment of Coronary Artery Diseases Trial - … | Phase4 | Acute Coronary Syndrome | Completed | 2014-07-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02173379 | Absorb IV Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2014-07-01 | 2022-04-06 | ClinicalTrials.gov |
| NCT02184117 | CONTRAST (Can cONTrast Injection Better Approximate FFR compAred to Pure reSTin… | — | Coronary Artery Disease | Completed | 2014-07-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02041702 | Accent Cardiac MRI Study | Na | Bradycardia | Completed | 2014-06-09 | 2016-03-17 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02404987 | An Oral Nutritional Supplement Study in Older Malnourished Spanish Population | — | Malnutrition | Unknown | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02132611 | Coronary Orbital Atherectomy System Study | Na | CAD | Completed | 2014-06-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02143791 | Evaluate St Jude Medical Prodigy Neuromodulation for FBSS or Chronic Pain of th… | Na | Chronic Pain | Completed | 2014-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02171065 | PROSPECT II & PROSPECT ABSORB - an Integrated Natural History Study and Randomi… | Na | Acute Coronary Syndrome (ACS) | Completed | 2014-06-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT02115269 | IndoProCaf Effervescent Tablets Effectiveness in Acute Treatment of Migraine an… | — | Headache Disorders, Primary | Completed | 2014-06-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02200029 | Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption | Phase3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | Completed | 2014-06-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02000115 | Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2014-05-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02146599 | Patient Perception of Visual Quality and Function | — | Cataract | Completed | 2014-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02189096 | Validation of Early Warning Score & Lactate in Prehospital Screening | — | Sepsis | Completed | 2014-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02229864 | Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery L… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02073071 | Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weig… | — | Other Preterm Infants | Completed | 2014-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02042300 | XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice | — | Percutaneous Transluminal Coronary Angioplasty | Completed | 2014-05-01 | 2024-08-30 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT01907828 | A Feasibility Study to Evaluate the Effect of Concomitant Renal Denervation and… | Na | Persistent Atrial Fibrillation | Completed | 2014-04-15 | 2018-10-15 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02672878 | Restenosis Intrastent: Bioresorbable Vascular Scaffolds Treatment (RIBS VI) | Phase4 | Coronary In-stent Restenosis | Unknown | 2014-04-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02125123 | Oral Nutritional Supplementation in Children | Na | Children | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT01993862 | Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Imp… | Na | Heart Failure | Completed | 2014-03-17 | 2016-08-12 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT03249610 | Randomized Control Trial for Overweight Employees in Worksites | Na | Diabetes Mellitus, Type 2 | Completed | 2014-03-11 | 2017-06-15 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02090387 | Evaluation of an Oral Nutritional Supplement on Lean Body Mass in Healthy Older… | Na | Healthy | Completed | 2014-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02089971 | Muscle Mass and Function in Chinese Adults | — | Sarcopenia | Completed | 2014-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02089906 | Health and Nutrition Status of Chinese Elderly | — | Malnutrition | Completed | 2014-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02086526 | Targeting Pathways in Polycystic Ovary Syndrome (PCOS) Using Metformin (MET) | Phase1 | Polycystic Ovary Syndrome | Completed | 2014-03-01 | 2016-11-20 | ClinicalTrials.gov |
| NCT02082184 | An Evaluation of a Novel Glucose Sensing Technology in Type 2 Diabetes | Na | Type 2 Diabetes Mellitus | Completed | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02064751 | MultiPoint Pacing Programming Guided by Noninvasive Hemodynamics | Na | Heart Failure | Completed | 2014-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02052232 | Study of Protein Metabolism in Healthy Older Subjects | Na | Malnutrition | Completed | 2014-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02030418 | The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker | Na | Bradycardia | Completed | 2014-02-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02057588 | Enhanced Diagnosis of Ventricular Activation Pattern Using Intracardiac Electro… | Na | Arrythmia | Completed | 2014-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02073058 | Evaluation of the Accuracy of the Abbott Sensor Based Interstitial Glucose Moni… | — | Type 1 Diabetes | Completed | 2014-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02069522 | Healthy Term Infants Fed Milk-Based Formulas | Na | Infants | Terminated | 2014-02-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02060760 | Use of Abbott High Sensitivity Troponin I Assay In Acute Coronary Syndromes | — | Acute Coronary Syndrome | Completed | 2014-02-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT01986803 | ABSORB STEMI: the TROFI II Study | Na | Acute ST Segment Elevation Myocardial Infarction | Completed | 2014-01-06 | 2017-09-21 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02043197 | Fevarin® Effectiveness in Treatment of Depression in Patients With Neurological… | — | Depression | Completed | 2014-01-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02028156 | Feeding Intolerance in Formula-Fed Infants | Na | Feeding Intolerance | Terminated | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02208700 | Efficacy of Oxepa Enteral Feeding in LTAC (Long Term Acute Care Hospital) Patie… | Na | Acute Lung Injury | Unknown | 2014-01-01 | — | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02137382 | A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect… | Phase3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | Completed | 2014-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02006069 | MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing | Na | Heart Failure | Terminated | 2013-12-01 | 2021-05-30 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02011893 | SUNBURST (Success Using Neuromodulation With BURST) Study | Na | Chronic Pain | Completed | 2013-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02570776 | UBT as a Diagnostic Tool for HP Prevalance | — | Dyspepsia | Unknown | 2013-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02004730 | Italian Diffuse/Multivessel Disease ABSORB Prospective Registry: IT-Disappears | Phase4 | Coronary Artery Disease | Unknown | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02016261 | Study to Evaluate Cognitive Functioning in Remitted Depression During Treatment… | Phase4 | Recurrent Depressive Disorder | Completed | 2013-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02029144 | Observational Study of Dydrogesterone in Cycle Regularization | — | Observational Study | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02051972 | The LEADLESS Observational Study | — | Indications for VVI(R) Pacemaker | Completed | 2013-12-01 | 2021-12-22 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT02066623 | Observational Study to Evaluate Short and Long-term Safety of the ABSORB Scaffo… | — | Coronary Artery Stenosis | Completed | 2013-11-08 | 2021-07-06 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02187757 | Study to Evaluate Efficacy and Safety of PreLipid® on Subjects With Higher Than… | Phase3 | Hyperlipidemia | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02046746 | The Effect of a Renal Specific Oral Nutritional Supplement on Nutritional Status | Na | Chronic Kidney Disease | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02016586 | Breastfeeding Intervention Study | Na | Breast Feeding | Completed | 2013-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02009410 | A Study to Assess the Effect of Creon® on Pancreatic Exocrine Insufficiency in … | Phase4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | Withdrawn | 2013-11-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02006758 | Observational Study of the EnligHTN Renal Denervation System in Europe | — | Uncontrolled Hypertension | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01988415 | New Treatment Algorithm to Reduce Spherical Aberration After LASIK Correction f… | Na | Myopia | Completed | 2013-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01990287 | SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study | Na | Failed Back Surgery Syndrome | Terminated | 2013-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01218919 | Post Market (Brio™ System) Deep Brain Stimulation (DBS) PD Study | — | Parkinson Disease | Withdrawn | 2013-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01903187 | EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hy… | Na | Hypertension | Terminated | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01962051 | AMPLATZER Cardiac Plug (ACP) Latin American Post Market Observational | — | Atrial Fibrillation | Withdrawn | 2013-10-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01891643 | PH III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to Tr… | Phase3 | Newly Diagnosed, Previously Untreated Multiple Myeloma | Terminated | 2013-09-30 | 2020-06-25 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01930214 | Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely… | — | Coronary Artery Disease | Completed | 2013-09-26 | 2017-06-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01913080 | The Health Log: A Randomized Clinical Trial | Na | Rheumatoid Arthritis | Completed | 2013-09-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01477320 | Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients. | Na | Gastrointestinal Hemorrhage | Completed | 2013-09-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02346383 | Optimal Stimulation Programming for Spinal Peripheral Neuromodulation | Na | Chronic Pain | Completed | 2013-09-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01871090 | Remote Device Interrogation In The Emergency Department | Na | Heart Disease | Completed | 2013-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01963286 | Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (I… | Na | Tachycardia | Completed | 2013-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01850030 | A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dyd… | Phase3 | Female Infertility | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02056275 | A Study of an Oral Nutrition Supplement (ONS) in Children. | Na | Growth | Completed | 2013-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01932944 | Accuracy Characterization Study | — | Type2 Diabetes | Completed | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01974986 | Rehydration Following Exercise-Induced Dehydration | Na | Dehydration Related to Exercise | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01917266 | Evaluation of Left Ventricular (LV) Lead Positioning Using MediGuide | — | Heart Failure | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01497717 | Efficacy of Humira in Behcet Patients With Arthritis | Phase3 | Arthritis; Behcet | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01894152 | XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm … | — | Angioplasty | Completed | 2013-07-01 | 2019-10-09 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01923740 | A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) … | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2019-03-07 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01852123 | High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syn… | Na | Acute Coronary Syndrome | Completed | 2013-06-10 | 2017-03-03 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850134 | Evaluation of a Nutritional Supplement for People With Type 2 Diabetes. | Na | Diabetes | Withdrawn | 2013-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT01716039 | Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With… | Phase2 | Ulcerative Colitis | Terminated | 2013-06-01 | 2016-07-18 | ClinicalTrials.gov |
| NCT02325973 | Assessing Microvascular Resistance Via IMR To Predict Cumulative Outcome in STE… | Na | Multi Vessel Coronary Artery Disease | Completed | 2013-06-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT01847105 | Assessing Patient Comfort With Two Different Multi-Purpose Disinfecting Solutio… | Na | Contact Lens Solution Toxicity | Unknown | 2013-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT02335229 | A Post Market Study to Assess the Spinal Modulation Dorsal Root Ganglion Stimul… | — | Chronic Post Surgical Pain | Terminated | 2013-06-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02166216 | The North Sea Race Endurance Exercise Study | — | Healthy | Active_Not_Recruiting | 2013-06-01 | 2034-06-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01902212 | Evaluation of an Oral Nutrition Supplement | Na | Gastrointestinal Tolerance | Completed | 2013-06-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01850251 | Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Musc… | Phase4 | Hip Fractures | Terminated | 2013-06-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT02513719 | XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveill… | — | Ischemic Heart Disease | Completed | 2013-05-13 | 2019-09-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01858636 | Post-Market Study of the St. Jude Medical Angio-Seal™ V-Twist Integrated Platfo… | — | Vascular Closure | Completed | 2013-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01856725 | MPP Programming Study | Na | Heart Failure | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01855412 | Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes | — | Peripheral Arterial Occlusive Disease | Completed | 2013-05-01 | 2019-04-11 | ClinicalTrials.gov |
| NCT01850810 | Evaluation of a Nutritional Product for People With Type 2 Diabetes | Na | Diabetes | Completed | 2013-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01842568 | Vascular Events In Surgery patIents cOhort evaluatioN - Cardiac Surgery | — | Vascular Death | Completed | 2013-05-01 | 2025-07-01 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT02349646 | A Post Market Cohort With the Spinal Modulation Neurostimulator System in Perip… | — | Peripheral Neuropathy | Terminated | 2013-04-25 | 2016-10-24 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01802788 | 5 Year Observation of Patients With PORTICO Valves | — | Aortic Valve Stenosis | Completed | 2013-04-16 | 2022-10-19 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT01844284 | AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japan… | Na | Coronary Artery Disease | Completed | 2013-04-01 | 2019-01-16 | ClinicalTrials.gov |
| NCT02346643 | A Post Market Evaluation of Chronic intractaBle paIN and the Efficacy of drG st… | — | Chronic Pain | Terminated | 2013-04-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01772108 | A Randomized Study of the MitraClip Device in Heart Failure Patients With Clini… | Na | Cardiovascular Diseases | Terminated | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01836146 | International First-in-Human Study of the EnligHTN Generation 2 System in Patie… | Na | Hypertension | Completed | 2013-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01782456 | Tolerance of an Oral Nutritional Supplement(ONS) | Na | Gastro-Intestinal Tolerance | Completed | 2013-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02335489 | A Post Market Cohort to Assess the Performance of the Spinal Modulation Neurost… | — | Chronic Neuropathic Pain | Terminated | 2013-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01820130 | Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure | Na | Heart Failure | Withdrawn | 2013-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02819401 | The Effects of a High-fiber Formula in Children With Failure to Thrive | — | GI Tolerance | Completed | 2013-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01705080 | IntErnational Long-term Follow-up Study of Patients With Uncontrolled HyperTens… | — | Hypertension | Terminated | 2013-01-17 | 2019-11-27 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01798043 | Impact of Septal Vs Apical Pacing on Right and Left Ventricular Performance | Na | Heart Block | Terminated | 2013-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01805154 | Advance Cardiac Resynchronization Therapy (CRT) Registry | — | Heart Failure | Completed | 2013-01-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01650298 | Safety Study on Stopping Anticoagulation Medication in Patients With a History … | Na | Atrial Fibrillation | Terminated | 2013-01-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01759251 | Effectiveness of Betaserc® (Betahistine Dihydrochloride) in Patients With Vesti… | — | Vertigo | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01769287 | EP Study of Patients Who Have Received Left Atrial Ablation Using High Intensit… | — | Atrial Fibrillation | Completed | 2013-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT02257801 | Effects of Lutein on Learning and Memory in Chronically Stressed Subjects and i… | Phase2 | Healthy But Chronically Stressed | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02786173 | Peripheral Registry of Endovascular Clinical Outcomes "The PRIME Registry" | — | Peripheral Arterial Disease | Completed | 2013-01-01 | 2021-11-05 | ClinicalTrials.gov |
| NCT01938391 | Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal | Na | Peripheral Artery Disease | Completed | 2013-01-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT01675479 | Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refr… | Na | Hyperopia | Completed | 2012-12-31 | 2016-10-31 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT02234830 | Randomized Comparison of ExoSeal® and Angio-Seal Vascular Closure Devices: The … | Na | Coronary Disease | Completed | 2012-12-21 | 2017-05-14 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01663896 | Observational Study of OCT in a Patients Undergoing FFR | — | Coronary Artery Disease | Completed | 2012-12-11 | 2015-10-01 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01675492 | Safety and Effectiveness of Wavefront-guided LASIK for the Correction of Mixed … | Na | Astigmatism | Completed | 2012-12-06 | 2016-11-22 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01703611 | Diabetes in India Nutrition Guidelines Study (DINGS) | Na | Type 2 Diabetes Mellitus | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01685047 | A Clinical Evaluation of ST Changes in a Group of Patients Having Ventricular A… | — | Coronary Artery Disease | Completed | 2012-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01694394 | Prevalence of Sub-Clinical Atrial Fibrillation Using an Implantable Cardiac Mon… | — | Atrial Fibrillation | Completed | 2012-12-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01754714 | Study to Investigate the Effects of Different Doses of S-adenosyl-L-methionine … | Phase3 | Non Alcoholic Fatty Liver Disease | Completed | 2012-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01746407 | Procurement of Human Specimens for the Evaluation of Early Markers of Sepsis | — | Infection | Completed | 2012-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01751906 | ABSORB III Randomized Controlled Trial (RCT) | Na | Coronary Artery Disease | Completed | 2012-12-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02146612 | Amino Acid Usage Patterns in Daily Practice | — | Wounds | Completed | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01418040 | PROstate Cancer Imaging, Treatment and Toxicity (PROCITT) | — | Prostate Cancer | Completed | 2012-11-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01731405 | Consumer Understanding and Use of Medication Guides | — | Revised Medication Guide Formats | Completed | 2012-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01722214 | Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Pso… | Phase4 | Psoriasis | Completed | 2012-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01714635 | Clinical Investigation of Expanded Designs of a Multifocal IOL | Phase1 | Cataract | Completed | 2012-11-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01713660 | Corneal Incisions With the IntraLase iFS Femtosecond Laser System | Na | Cataract | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01690598 | Veliparib and Topotecan for Relapsed Ovarian Cancer With Negative or Unknown BR… | Phase1 | Ovarian Cancer | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02169401 | A Multi-centre Observational Study of the Axium Neurostimulator as a Treatment … | — | Chronic Pain | Completed | 2012-11-01 | 2017-01-25 | ClinicalTrials.gov |
| NCT01749618 | Closing the Gap in Care in Seronegative Inflammatory Arthritis | Na | SpA | Completed | 2012-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01747668 | Lactation Fortification Study | Phase3 | Lactation | Completed | 2012-11-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01733368 | QUARTO-II Study to Evaluate the Management of Patients Resynchronized With the … | — | Heart Failure | Completed | 2012-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01730898 | Lutein Absorption in Healthy Adults | Phase3 | Healthy Subjects | Completed | 2012-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01609205 | Doppler Evaluation in RA Patients After Adalimumab. | Phase4 | Rheumatoid Arthritis | Completed | 2012-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01713348 | Sensor and Software Use for Improved Glucose Control in MDI Managed Diabetes | Phase4 | Diabetes Mellitus | Completed | 2012-10-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01720368 | OPERA Database - Crohn's Protocol | — | Inflammatory Bowel Disease | Completed | 2012-10-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT02981004 | PAR I - Patient-to-Annulus Relation I | — | Aortic Valve Disease | Completed | 2012-10-01 | 2017-12-18 | ClinicalTrials.gov |
| NCT01626404 | Screening for Advanced Heart Failure Treatment (SEE-HF) | — | Advanced Heart Failure | Completed | 2012-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01781624 | Evaluation of an Oral Nutritional Supplement | Na | Gastro-intestinal Tolerance | Completed | 2012-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01562951 | Assessment of Mucosal Activity to Improve the Prognosis of Patients With Crohn'… | Phase3 | Crohn's Disease | Terminated | 2012-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01721096 | XIENCE PRIME Japan Post-Marketing Surveillance (PMS) | — | Angina | Completed | 2012-10-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01673256 | DEtermining Accuracy and TrEnding CharacTerization of AF | — | Atrial Fibrillation | Completed | 2012-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01464502 | Pressure Wire Guided Cardiac Resynchronisation Therapy | Phase2 | Heart Failure | Unknown | 2012-09-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02227758 | Peripheral Nerve Stimulation Registry for Intractable Migraine Headache | — | Intractable Chronic Migraine | Completed | 2012-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01705873 | Analysis on the Risk of Cardiovascular Events in HIV- Infected Subjects Treated… | — | HIV | Unknown | 2012-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01711216 | Treatment Regimen in Menstrual Cycle Regularization and Persistence in Routine … | — | Irregular Menstrual Cycle | Completed | 2012-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01642186 | Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide… | Phase2 | Fibrolamellar Carcinoma | Completed | 2012-07-12 | 2021-07-16 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01593917 | Trifecta™ Long Term Follow-Up (LTFU) Study | — | Aortic Valve Insufficiency | Completed | 2012-07-02 | 2019-09-26 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01436747 | Efficacy and Safety of Paricalcitol for Reduction of Proteinuria in Kidney Tran… | Phase3 | Disorder of Transplanted Kidney | Completed | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01629160 | Ventricular Wall Motion Characterization | — | Atrial Fibrillation | Completed | 2012-07-01 | — | ClinicalTrials.gov |
| NCT01629628 | Adalimumab for the Management of Post-operative Crohn's Disease (CD) | Phase3 | Crohn Disease | Unknown | 2012-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01678781 | Open International Study on Quality of Life in Irritable Bowel Syndrome (IBS) P… | — | Irritable Bowel Syndrome | Completed | 2012-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01776567 | Apposition Assessed Using Optical Coherence Tomography of Chromium Stents Eluti… | Phase4 | Coronary Artery Disease | Unknown | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01633749 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Prophylaxis of Influenza | Completed | 2012-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02630667 | The Acute Effects Fortified Nutritional Supplementation on Childhood Cognition | Na | Cognitive Ability, General | Completed | 2012-06-01 | — | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01564173 | Dependence of LV Hemodynamics on Pacing Site | — | Heart Failure | Completed | 2012-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01674712 | A 12-week Study to Compare the Efficacy and Safety of Fixed Combinations of Fen… | Phase3 | Dyslipidemia | Completed | 2012-06-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01669655 | Plasma Profile of Exclusively Breastfed Infants | — | Breast Fed Infants | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01647360 | Severity of Bleeding as a Predictor of Quality of Life (QoL) in Women With Heav… | — | Menorrhagia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01631227 | Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressur… | Phase3 | Essential Hypertension | Completed | 2012-06-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01747330 | Evaluation of Safety and Tolerability of Creon Micro in Children Younger Than F… | Phase3 | Pancreatic Exocrine Insufficiency | Completed | 2012-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01614405 | Highly Active Antiretroviral Therapy for Patients With Primary Biliary Cirrhosis | Na | Primary Biliary Cirrhosis | Terminated | 2012-06-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01608100 | Evaluation of a New Cardiac Biomarker Assay | Phase3 | Acute Coronary Syndrome | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01582139 | Feasibility Study of Closed Loop Control in Type 1 Diabetes Using Heart Rate Mo… | Na | Type 1 Diabetes Mellitus | Completed | 2012-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01485666 | Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Manageme… | — | Left Ventricular Assist Device | Completed | 2012-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01667068 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 7.5 Years Fol… | — | Coronary Heart Disease | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01525563 | Duphaston in Cycle Regularization: A Post-marketing, Prospective, Multicenter, … | — | Irregular Menstrual Cycle | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01583608 | ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting B… | — | Cardiovascular Diseases | Completed | 2012-04-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01564186 | Characterization of Cardiac Hemodynamics During MultiSite Pacing | — | Heart Failure | Completed | 2012-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02335502 | A Post Market Study to Assess the Spinal Modulation Neurostimulator System for … | — | Chronic Pain | Completed | 2012-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01556672 | Adalimumab-psoriasis and Small Bowel Lesions | Phase4 | Plaque Psoriasis | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01576016 | Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker a… | Na | Adverse Effect of MRI on an Implanted Pacemaker Lead | Completed | 2012-03-30 | 2018-02-02 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01562613 | A Blood Pressure Regulation and Stroke Risk Evaluation Study in Hypertensive Pa… | — | Hypertension | Completed | 2012-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01656278 | An MRI-guided Treatment Strategy to Prevent Disease Progression in Patients Wit… | Na | Arthritis | Completed | 2012-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01648777 | Catheter Outcomes With Sternotomy Cardiac Operated | Phase3 | Pneumonia | Completed | 2012-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01835808 | Portuguese Study on The Evaluation of FFR Guided Treatment of Coronary Disease | — | Coronary Artery Disease | Completed | 2012-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01522352 | Comparison Between Three Types of Stented Pericardial Aortic Valves | Na | Aortic Valve Replacement | Unknown | 2012-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01555619 | Quadripolar Pacing Post Approval Study | — | Heart Failure | Completed | 2012-02-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01468285 | The CBF Study Evaluating the Effect of Betahistine on the Cerebral Blood Flow | Phase4 | Gait or Balance Disorder Problems | Completed | 2012-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01602822 | Safety and Acceptability Study of Non-occupational Prophylaxis (PEP) Following … | Phase4 | HIV | Terminated | 2012-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01550835 | Impact of Aspiration Thrombectomy During Carotid Stenting | Na | Carotid Artery Stenosis | Unknown | 2012-02-01 | — | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01528150 | Safety and Efficacy Study of Tendril MRI™ Leads in Standard Bradycardia Pacing … | — | Bradycardia | Completed | 2012-02-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01573871 | Tolerance and Compliance of Infants Fed an Hydrolyzed Infant Formula | Phase3 | Infant | Completed | 2012-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01842243 | Effect of Septal Versus Apical Pacing- a Comparative Study Using Cardiac MRI | Na | Ventricular Dysfunction | Completed | 2012-02-01 | 2015-12-31 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01489761 | LONG-DES VI (Drug Eluting Stent for Long Lesions in Coronary Artery) | Phase4 | Coronary Artery Disease | Terminated | 2012-01-01 | 2017-02-14 | ClinicalTrials.gov |
| NCT01519466 | Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Stu… | Na | Type 1 Diabetes | Completed | 2012-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01519739 | Clinical Evaluation of Mediguide System in Cardiac Resynchronization Therapy (C… | Na | Heart Failure | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01535404 | Right Versus Left Apical Transvenous Pacing for Patients With Preserved Left Ve… | Na | Bradyarrhythmia | Terminated | 2012-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01500148 | St. Jude Medical Percutaneous Mitral Valve Repair Study | Phase1 | Mitral Valve Prolapse | Completed | 2011-12-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01716884 | China STEMI-PCI Program | — | ST Segment Elevation Myocardial Infarction | Unknown | 2011-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02377596 | Assessment of a Feeding Difficulties Diagnostic Tool Questionnaire For Children… | — | Feeding Difficulties | Withdrawn | 2011-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01663168 | EARNEST Rifabutin Pharmacokinetics (PK) Substudy | Phase2 | HIV | Unknown | 2011-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01588691 | Traumatic Brain Injury Peripheral Nerve Study | Phase1 | Traumatic Brain Injury | Completed | 2011-12-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01468974 | ESPRIT I: A Clinical Evaluation of the Abbott Vascular ESPRIT BVS (Bioresorbabl… | Na | Atherosclerosis | Completed | 2011-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01472783 | Veliparib Monotherapy for Relapsed Ovarian Cancer With BRCA Mutation | Phase1 | Recurrent, Epithelial Ovarian Cancer | Completed | 2011-11-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01425281 | ABSORB II Randomized Controlled Trial | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2018-05-23 | ClinicalTrials.gov |
| NCT01341340 | The ABSORB BTK (Below The Knee) Clinical Investigation | Na | Atherosclerosis | Terminated | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01408485 | Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter | Na | Typical Atrial Flutter | Completed | 2011-11-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01510652 | More Options Available With a Quadripolar LV Lead pRovidE In-clinic Solutions t… | Na | Postoperative Cardiac Complication | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01464320 | A Study to Evaluate the Safety and Tolerability of ABT-614 and Its Effect on Ki… | Phase1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | Completed | 2011-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01484613 | Selected Site Pacing to Avoid Phrenic Nerve Stimulation in Cardiac Resynchroniz… | — | Heart Failure | Completed | 2011-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01301625 | MitraClip System in Australia and New Zealand | — | Mitral Regurgitation | Terminated | 2011-11-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01482845 | A Phase 1 Study of the Safety, Tolerability and Pharmacokinetics of ABT-126 in … | Phase1 | Alzheimer's Disease | Completed | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01477528 | Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the He… | — | Anticoagulation | Completed | 2011-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01476020 | Is There A LIfe for Drug Eluting Stent (DES) After Discontinuation of Clopidogr… | — | Restenosis | Unknown | 2011-11-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01658267 | Compliance With Dietary Recommendations in Children at Risk for Undernutrition | Phase3 | Children | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00969865 | Individualized Comprehensive Atherosclerosis Risk-reduction Evaluation Program | — | Atherosclerosis | Completed | 2011-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01448135 | Tolerance and Efficacy of a Predigested, High Protein, High Omega 3 Fat Enteral… | Na | Critical Illness | Completed | 2011-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01462877 | A Study to Evaluate Fenofibrate Combination With Statin in Chinese Patients Wit… | Phase4 | Dyslipidemias | Completed | 2011-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01464385 | Nutrition Beverage Tolerance Study | Phase2 | Human Volunteers | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01476956 | Assess Structural Damage in Rheumatoid Arthritis Using Biomarkers and Radiograp… | — | Rheumatoid Arthritis | Completed | 2011-10-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT01444378 | Absolute Pro® MOMENTUM™ | Na | Peripheral Artery Disease | Completed | 2011-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01483976 | Comparison of Medical Nutritional Supplements | Phase3 | Elderly | Completed | 2011-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01495351 | Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients W… | Phase1 | Multiple Myeloma | Completed | 2011-10-01 | 2015-02-10 | ClinicalTrials.gov |
| NCT01438229 | Safety and Efficacy Study of Renal Artery Ablation in Resistant Hypertension Pa… | Na | Hypertension | Completed | 2011-10-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01401361 | Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along Wi… | Phase3 | Typical Atrial Flutter | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01764334 | Fractional Flow Reserve Versus Angiographically Guided Management to Optimise O… | Phase4 | NonST Elevation Myocardial Infarction | Unknown | 2011-10-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01477723 | Evaluation of an Oral Nutritional Supplement in Older Hospitalized Patients | Phase3 | Pneumonia | Terminated | 2011-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01506934 | A Study Evaluating the Bioavailability of Two Formulations of Linifanib and Foo… | Phase1 | Advanced or Metastatic Solid Tumors | Terminated | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01536236 | Spinal Cord Stimulation for Diabetic Polyneuropathy | Na | Diabetic Polyneuropathy | Withdrawn | 2011-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01435031 | EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Elut… | Na | Coronary Artery Disease (CAD) | Completed | 2011-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01432275 | Ease of Use of New Blood Glucose Meter With In-built Insulin Calculator at Home… | Na | Diabetes Mellitus | Completed | 2011-09-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01573884 | Ex Vivo Exploratory Analysis in Healthy Full-term Infants | — | Healthy Infant and Mother Pairs | Completed | 2011-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01393808 | Salt Intake and Antiproteinuric Effect of Paricalcitol in Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2011-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01286974 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes Linifanib in… | Phase1 | Advanced Solid Tumors | Terminated | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01482507 | Examination of the Effectiveness of Diffusion Weighted Magnetic Resonance Imagi… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01527344 | Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography | — | Cardiac Allograft Vasculopathy | Completed | 2011-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01421680 | The Effects of Preoperative and Postoperative Oral Nutritional Supplements in M… | Na | Malnourished | Completed | 2011-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01373073 | Evaluation of a Novel Human Milk Fortifier in Preterm Infants | Phase3 | Preterm Infants | Completed | 2011-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01299207 | PITT PCI Xience Registry | — | Coronary Artery Disease | Completed | 2011-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01487330 | First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System | Na | Symptomatic Aortic Stenosis | Completed | 2011-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01377103 | Testosterone Therapy in Heart Failure | Na | Heart Failure | Withdrawn | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01276093 | Pulmonary Vein Ablation Versus Amiodarone in the Elderly | Na | Atrial Fibrillation | Terminated | 2011-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01288352 | Early Treatment of Atrial Fibrillation for Stroke Prevention Trial | Phase4 | Atrial Fibrillation | Completed | 2011-07-01 | 2020-05-31 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01385826 | Effect of Adalimumab for the Treatment of Uveitis in Juvenile Idiopathic Arthri… | Phase2 | Uveitis | Completed | 2011-06-29 | 2015-08-27 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01366144 | Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors T… | Phase1 | Breast Carcinoma | Active_Not_Recruiting | 2011-06-20 | 2027-03-03 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01801319 | A Clinical Evaluation of Subcallosal Cingulate Gyrus Deep Brain Stimulation for… | Na | Treatment Resistant Depression | Unknown | 2011-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT04154852 | ADalimumab in Persistent Early Oligoarthrits Study (ADEOS) | Phase2 | Oligoarthritis | Completed | 2011-06-01 | 2017-01-16 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01393041 | St. Jude Medical Angio-Seal VIP Vascular Closure Device | Na | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01390610 | Continuous Glucose Monitoring Self-Monitored Blood Glucose Type 2 Therapy Matri… | — | Diabetes Mellitus, Type 2 | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387009 | Acquisition of Normative Data for Musculoskeletal Ultrasound in Children | — | Normative Data Study of Joints of Healthy Children | Completed | 2011-06-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01380886 | Growth and Tolerance of Young Infants Fed Infant Formulas | Phase3 | Infant Newborn | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01366404 | Study of the Natural History of FFR Guided Percutaneous Coronary Intervention | — | Coronary Artery Disease | Recruiting | 2011-06-01 | 2037-04-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01401933 | Effect of Rifampin on the Pharmacokinetics of Linifanib in Subjects With Advanc… | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01405326 | REstore Working Ability in RheumatoiD Arthritis | Phase4 | Rheumatoid Arthritis | Unknown | 2011-05-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01381341 | To Compare Relative Bioavailability of Two Clinical Formulations of Linifanib. | Phase1 | Advanced Solid Tumors | Completed | 2011-05-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01545310 | A Positron Emission Tomography Study of SLV354 in Healthy Subjects and Subjects… | Phase1 | Schizophrenia | Completed | 2011-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01354938 | Outcome Study to Evaluate Klaricid XL® (Clarithromycin Modified Release) in Pat… | — | Bronchitis | Completed | 2011-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01352819 | Post Market (Libra/LibraXP System) Deep Brain Stimulation (DBS) Parkinson's Dis… | — | Parkinson's Disease | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01348854 | Safety and Effectiveness of Arcuate Incisions Performed With the iFS Femtosecon… | Phase2 | Corneal Astigmatism | Completed | 2011-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01331330 | European Deep Brain Stimulation (DBS) Depression Study | Na | Depressive Disorder, Major | Completed | 2011-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01192035 | PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial | Phase4 | HIV-1 | Completed | 2011-05-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01605721 | Efficacy and Safety of Xience in Coronary arEry Disease aLL-comers After stENTi… | Phase4 | Coronary Artery Disease | Unknown | 2011-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01338740 | Switching From Adalimumab to Infliximab | — | Crohn's Disease | Completed | 2011-04-01 | 2014-02-17 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01348399 | Evaluation of Effectiveness and Safety of XIENCE PRIME Stent (IRIS-PRIME) | — | Coronary Artery Disease | Completed | 2011-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01362725 | Spinal Cord Stimulation For Heart Failure | Phase2 | Systolic Heart Failure | Completed | 2011-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01260844 | Open Label, Single Dose, Non-randomized Study to Assess the Drug to Drug Intera… | Phase1 | Moderate to Severe Plaque Psoriasis | Withdrawn | 2011-04-01 | — | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01346319 | Study of the Safety, Tolerability and Pharmacokinetics of Testosterone Undecano… | Phase1 | Hypogonadal Males | Completed | 2011-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01282086 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01294228 | Rapid Evaluation of Acute Kidney Injury With NGAL in Acutely Ill Patients in th… | — | Acute Kidney Injury | Completed | 2011-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01295814 | Efficacy Study of Adalimumab to Treat Interstitial Cystitis | Phase3 | Interstitial Cystitis | Completed | 2011-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01617889 | Healthy Term Infants Fed Milk-Based Formulas | Phase3 | Healthy Term Infant | Completed | 2011-03-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01214408 | Effect of Digene Total (Buffered Pantoprazole) on 24 Hour Gastric Potential Hyd… | Phase4 | Acid Peptic Disorder | Completed | 2011-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01604902 | miRNAs and mRNAs in Psoriasis | — | Psoriasis | Unknown | 2011-03-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01337999 | Human Epididymis Protein 4 in Normal Menstruating Women | — | Healthy Premenopausal Women | Unknown | 2011-03-01 | — | ClinicalTrials.gov |
| NCT01294839 | Right Ventricular Outflow Tract Study | Na | Sinus-node Dysfunction | Completed | 2011-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01258218 | Accent MRI Pacemaker and Tendril MRI Lead New Technology Assessment | — | Bradycardia | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT02052765 | AnalyST & Brugada Syndrome - Feasibility Study | Na | Brugada Syndrome | Completed | 2011-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01294917 | Comparison of a New Abbott Medical Optics (AMO) Multi-Purpose Solution (MPS) to… | Na | Normal Contact Lens Wearers | Completed | 2011-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01191125 | Evaluation of an Oral Nutritional Supplement Containing AN777 | Phase3 | Malnutrition | Completed | 2011-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT02242578 | Treating Refractory Schizophrenia With rTMS | Na | Schizophrenia | Terminated | 2011-01-24 | 2018-06-11 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01489865 | ABT-888 With Modified FOLFOX6 in Patients With Metastatic Pancreatic Cancer | Phase1 | Metastatic Pancreatic Cancer | Completed | 2011-01-03 | 2023-12-07 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01295840 | Quartet Lead and Resynchronization Therapy Options | Phase4 | Heart Failure | Completed | 2011-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01075204 | Clarithromycin Modified Release Observational Study for Evaluation of Treatment… | — | Respiratory Tract Infection | Completed | 2011-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01191112 | Evaluation of the Safe Use and Tolerance of a Peptide-based Formula in a Pediat… | Phase3 | Gastrointestinal Diseases | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01283126 | Blood/Interstitial Glucose Measurements and Cognitive Function During Hypoglyce… | Na | Hypoglycemia | Completed | 2011-01-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01275508 | Safety and Tolerability of FITC-Adalimumab Administration During Confocal Laser… | Phase1 | Crohn's Disease | Completed | 2011-01-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01292317 | Neutrophil Gelatinase-associated Lipocalin (NGAL) and Contrast Media Induced Ne… | Na | Contrast Media Induced Nephropathy (CIN) | Completed | 2011-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01256710 | Trifecta™ Durability Study | — | Aortic Valve Disease | Terminated | 2011-01-01 | 2021-03-12 | ClinicalTrials.gov |
| NCT01278953 | TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation | Na | Paroxysmal Atrial Fibrillation | Completed | 2011-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01234727 | Comparison Study of Blood Glucose Monitoring Systems in People With Diabetes | — | Diabetes Mellitus | Completed | 2010-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01237444 | Study of Lopinavir/ Ritonavir and Lamivudine Versus Standard Therapy in Naïve H… | Phase3 | HIV Infection | Completed | 2010-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01291836 | Acute Kidney Injury Neutrophil Gelatinase-Associated Lipocalin Evaluation of Sy… | — | Acute Decompensated Heart Failure | Completed | 2010-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01271816 | Prolonged Monitoring to Detect Ventricular Arrhythmias in Presymptomatic Arrhyt… | — | Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) | Terminated | 2010-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01275118 | Comparison of Postoperative Visual Acuity and Spectacle Independence Between th… | Phase4 | Cataract | Completed | 2010-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT02131337 | TactiCath® Prospective Effectiveness Pilot Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01203748 | Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial - Sta… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01580124 | CatHeter Ablation of perSistEnd Atrial Fibrillation: Pulmonary Vein Isolation V… | Na | Atrial Fibrillation | Completed | 2010-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01191476 | Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas… | Phase4 | Elective Laparoscopic Surgery | Completed | 2010-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01214824 | Use of the FreeStyle Navigator Continuous Glucose Monitoring System to Enhance … | Na | Diabetes Mellitus | Completed | 2010-11-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01249027 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval,… | — | Angioplasty | Completed | 2010-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01205789 | EXCEL Clinical Trial (Universal Registry) | — | Chronic Coronary Occlusion | Completed | 2010-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00935480 | IntensVIH: Impact Of Therapy Intensification By An Integrase Inhibitor +/- CCR5… | Phase3 | HIV Infections | Completed | 2010-10-01 | 2014-08-08 | ClinicalTrials.gov |
| NCT01222104 | Angio-Seal Interventional Radiology (IR) Registry | — | Diagnostic and/or Interventional Radiology Procedures | Completed | 2010-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01172990 | Direct Angioplasty for Non ST Elevation Acute Coronary Events: DANCE Pilot Study | Na | Acute Coronary Syndrome | Terminated | 2010-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01641770 | Oral Nutritional Supplementation in Hospital Patients | Phase3 | Malnutrition | Completed | 2010-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01197144 | Pain Modulation in Rheumatoid Arthritis (RA) - Influence of Adalimumab | Na | Arthritis, Rheumatoid | Completed | 2010-10-01 | 2016-11-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01205776 | EXCEL Clinical Trial | Na | Chronic Coronary Occlusion | Completed | 2010-09-29 | 2019-06-28 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01179477 | QuickFlex Micro Left Ventricular Lead Post Approval Study | — | Heart Failure | Completed | 2010-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01199471 | Estimate the Behavior of Chinese Anesthesiologists Practicing General Anesthesi… | — | Anesthesia, General | Completed | 2010-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01190969 | A Trial of Oral Nutritional Supplements on Nutritional Status and Clinical Outc… | Na | Malnutrition | Withdrawn | 2010-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01204528 | Vitamin-D Receptor Activation (VDRA) in Chronic Kidney Disease | Phase2 | Chronic Kidney Disease | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01181570 | Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sl… | Phase4 | Psoriasis | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01205854 | Aiming for Remission in Rheumatoid Arthritis (RA) - the ARCTIC Trial | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01240122 | Short-Term Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mult… | Na | Corneal Staining | Completed | 2010-08-31 | 2010-11-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01186198 | A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter … | — | Ischemic Heart Disease | Completed | 2010-08-12 | 2010-12-30 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01278030 | Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selecti… | Na | Heart Failure | Completed | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01181427 | Study of ABT-267 in Both Healthy Volunteers and Hepatitis C Virus (HCV) Genotyp… | Phase1 | HCV Infection | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01178268 | XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval … | Phase4 | Coronary Occlusion | Completed | 2010-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01163162 | The Effect of Paricalcitol on Creatinine Filtration, Secretion and Glomerular F… | Phase4 | Chronic Kidney Disease | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01205828 | ABT-888 and Temozolomide for Liver Cancer | Phase2 | Hepatocellular Carcinoma | Terminated | 2010-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01124851 | Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of ABT-652 in S… | Phase1 | Sleep Disorder | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01097330 | Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Pati… | Phase3 | Defibrillators, Implantable | Terminated | 2010-08-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01326299 | Post Prandial Glucose Control Proof-of-Principle | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01324921 | Effect of Nutritional Products on Metabolic Parameters in Subjects With Type 2 … | Phase2 | Diabetes Mellitus, Type 2 | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01138475 | Trial Of Paricalcitol and Cholecalciferol(Vitamin D3) in the Treatment Of Secon… | Phase3 | Gastric Bypass | Completed | 2010-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01074749 | Optimal Sensing in Atrial Tachyarrhythmia's Study | Na | Sick Sinus Syndrome | Terminated | 2010-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01176201 | 14-C ADME (Absorption, Disposition, Metabolism and Excretion) Study in Man | Phase1 | Healthy Subjects | Completed | 2010-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01193140 | To Evaluate the Safety of Veliparib in Combination With Temozolomide in Subject… | Phase2 | Solid Tumor Cancers | Completed | 2010-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01266239 | Comparison Between Everolimus-eluting Stent (EES) and Sirolimus-eluting Stent (… | Na | Ischemic Heart Disease | Unknown | 2010-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01210820 | Feasibility of iFS™ for Intrastromal Arcuate Keratotomy (ISAK) Procedures | Na | Refractive Astigmatism | Completed | 2010-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01298609 | Occipital Nerve (C2) Stimulation in the Treatment of Fibromyalgia | Na | Fibromyalgia | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01146015 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2010-06-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01226095 | Evaluation of the Effectiveness, Compliance of Ibuprofen in a Sustained Release… | — | Osteoarthritis | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01105741 | Metabolomic Analysis, a Potential Tool to Direct Treatment With Adalimumab in C… | — | Crohn's Disease | Completed | 2010-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01176045 | TearLab Refractive Surgery Dry Eye Study | — | Dry Eye Syndromes | Completed | 2010-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01160328 | Influence of Male Hormones on Regional Fat Metabolism | Phase1 | Obesity | Completed | 2010-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01137877 | Growth and Tolerance of Healthy Term Infants to a New Infant Formula | Phase3 | Healthy Term Infants | Terminated | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01126619 | A Study of Effectiveness and Safety of Tumor Necrosis Factor (TNF) Inhibitors i… | — | Psoriasis | Completed | 2010-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01114191 | A Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of Linifan… | Phase1 | Solid Tumors | Completed | 2010-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01172067 | QuickOpt Chronic Study | Na | Heart Failure | Completed | 2010-05-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01093001 | Tricuspid Regurgitation Study | Phase4 | Tricuspid Regurgitation | Completed | 2010-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01132495 | FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Interventi… | Na | Coronary Artery Disease | Completed | 2010-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01118299 | AMPLATZER Cardiac Plug Clinical Trial | Na | Atrial Fibrillation | Completed | 2010-04-26 | 2018-12-06 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01070069 | Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial | Na | Abdominal Aortic Aneurysm | Completed | 2010-04-13 | 2012-09-05 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01115933 | A Clinical Evaluation of the XIENCE PRIME Small Vessel Everolimus Eluting Coron… | Na | Vascular Disease | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01121107 | Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy | Na | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01090076 | The Use of Specialised Amino Acid Mixture in Pressure Ulcer Wound Healing Rates… | Na | Pressure Ulcer | Completed | 2010-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01127139 | Effectiveness and Patient Self-assessed Compliance of Blood Pressure Treatment … | — | Essential Hypertension | Completed | 2010-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01068873 | Kaletra and Maraviroc in Antiretroviral Therapy (ART)-Naive Patients (KALMAR St… | Phase4 | HIV Infections | Terminated | 2010-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01331317 | Effect of a Vitamin D Analogue vs Placebo on p-NT-proBNP in Patients With Type … | Phase4 | Cardiovascular Disease | Completed | 2010-04-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01464853 | Effect of Enteral Nutrition Support for Critically Ill Patients | Phase3 | Respiratory Distress Syndrome,Adult | Terminated | 2010-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01134913 | Multi-Markers In the Diagnosis of Acute Coronary Syndrome | — | Acute Coronary Syndrome | Completed | 2010-03-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00918450 | Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chro… | Phase2 | B-cell Chronic Lymphocytic Leukemia | Withdrawn | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01086228 | XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Pro… | — | Angina | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01155414 | Tolerance of Healthy Term Infants Fed Infant Formulas #4 | Phase3 | Healthy Term Infants | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01108185 | Evaluation of the Treatment With Klacid®SR in Patients With Lower Respiratory T… | — | Tracheitis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01300000 | Effects of Early Nutrition on Growth | Na | Infant Newborn | Completed | 2010-03-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00941564 | Comparative Ca Absorption and Tolerance in Healthy Term Infants Fed Milk-based … | Phase4 | Infant | Completed | 2010-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01081483 | A Study of Single Doses of ABT-072 in Japanese Healthy Male Adults | Phase1 | Hepatitis C | Completed | 2010-03-01 | — | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01069172 | Study of the Femtosecond Laser System as Compared to Continuous Curvilinear Cap… | Phase3 | Cataract | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01072565 | Modal Day Analysis of Self Monitoring Blood Glucose Versus Continuous Glucose M… | Na | Type 2 Diabetes | Completed | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01091649 | Study in Healthy Adults to Evaluate the Bioavailability of Two Test Tablet Form… | Phase1 | Healthy | Completed | 2010-02-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01130883 | Evaluation of Effectiveness of the Treatment After Repeated Administration of K… | — | Tracheitis | Completed | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01133574 | This is a Single Ascending Dose Tolerance Study | Phase1 | Cognition Disorders | Terminated | 2010-02-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01144598 | Time to DMARD (Disease-Modifying Anti-Rheumatic Drug) Treatment and Actual Work… | — | Rheumatoid Arthritis | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00907231 | Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in … | — | Acute Myocardial Infarction | Withdrawn | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01200160 | Study of the Effectiveness and Safety of Niaspan ® in the Treatment of Lipid Ab… | — | Cardiovascular Diseases | Completed | 2010-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01464866 | Effect of Nutritional Supplementation on Pediatric Burn Patients | Phase3 | Burns | Completed | 2010-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00996086 | Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT) | — | Heart Failure | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01044472 | Multi-site Left Ventricular (MSLV) Pacing With Quartet 1458Q Lead | — | Multi-site Left Ventricular Pacing | Completed | 2010-02-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01044784 | Acute Evaluation of the Safety of Left Ventricular-left Ventricular (LV-LV) Del… | — | Cardiac Resynchronization Therapy | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01056328 | Irrigated Ablation System Evaluation for Atrial Fibrillation (AF) | Na | Paroxysmal Atrial Fibrillation | Completed | 2010-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01062126 | BRADYCARE: Advanced Bradycardia Device Feature Utilization and Clinical Outcomes | — | Pacemaker | Completed | 2010-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01067716 | Performance and Acceptability of VSS-R | Na | Refractive Error | Completed | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00985478 | First in Man Study With SLV342 | Phase1 | Pharmacokinetics | Terminated | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00999206 | Study Measuring the Safety, Immunogenicity and Lot Consistency of Cell Derived … | Phase3 | Influenza | Completed | 2010-01-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01114880 | Efficacy and Safety of Adalimumab in Adult Chinese Subjects With Active Ankylos… | Phase3 | Ankylosing Spondylitis | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00936195 | Universal Use of EFV-TDF-FTC and AZT-3TC-LPV/r Combinations for HIV-1 PMTCT in … | Phase3 | HIV Infection | Withdrawn | 2010-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01009593 | Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellula… | Phase3 | Hepatocellular Carcinoma Non-resectable | Terminated | 2010-01-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01012414 | Effect of Vitamin D Supplement on Inflammation Markers in High-Risk Cardiovascu… | Phase3 | Coronary Artery Disease | Terminated | 2010-01-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01021358 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navi… | Phase1 | Lymphoma | Completed | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01390259 | Hypoglycemia Prevention After Exercise in Adolescent T1DM Patients Using a Cont… | Na | Type 1 Diabetes Mellitus | Completed | 2010-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01239953 | RIBS V (Restenosis Intra-stent of Bare Metal Stents: Paclitaxel-eluting Balloon… | Phase4 | In-Stent Restenosis | Unknown | 2010-01-01 | — | ClinicalTrials.gov |
| NCT01023789 | ABSORB EXTEND Clinical Investigation | Na | Myocardial Ischemia | Completed | 2010-01-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01030809 | Trial of a Treatment Algorithm for the Management of Crohn's Disease | Phase4 | Crohn's Disease | Completed | 2010-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01828970 | Pilot Study of Glycemic Control in Diabetic Hemodialyzed Patients | Phase4 | Diabetes Mellitus | Completed | 2010-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01045369 | A Pilot Study of Kaletra and Intelence Tablets in Naive Subjects | Phase4 | HIV Infections | Completed | 2010-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01196273 | Cardiovascular Diseases in HIV-infected Patients HIV-HEART Study: 5 Years Follo… | — | Coronary Heart Disease | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01126567 | Exploratory Biomarker Study of Cerebrospinal Fluid in Healthy Volunteers | — | Healthy | Completed | 2009-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01050127 | A Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multi… | Phase1 | Healthy | Completed | 2009-12-01 | — | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02018133 | Identification of Markers for Determining the Efficacy of Vitamin D Receptor Ac… | — | CKD Stage 3/4 | Completed | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01058980 | ADenosine Following Pulmonary Vein Isolation to Target Dormant Conduction Elimi… | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2009-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00924534 | A Safety PK/PD Study of SLV337 in Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes | Completed | 2009-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01132274 | Radiation Exposure Reduction in Supraventricular Tachycardia Ablation | Phase4 | Supraventricular Tachycardias | Completed | 2009-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01075516 | Health Economic Evaluation of Remote Follow up for Implantable Cardioverter Def… | — | Complication of Cardiac Defibrillator | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01188200 | Four-Hour Evaluation of a Medical Food in Subjects With Type 2 Diabetes | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2009-12-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01019564 | Complete Easy Rub Comparative Efficacy Study | Na | Myopia | Withdrawn | 2009-12-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00981318 | Pilot Assessment of Lopinavir/Ritonavir and Maraviroc | Phase4 | HIV Infections | Terminated | 2009-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00911508 | Catheter Ablation vs Anti-arrhythmic Drug Therapy for Atrial Fibrillation Trial | Na | Atrial Fibrillation | Completed | 2009-11-13 | 2017-12-31 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01013675 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Elderly | Phase2 | Influenza Vaccines | Completed | 2009-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00945581 | Evaluation of AN777 on Elderly Subjects During Bed Rest and Recovery | Phase1 | Aged | Completed | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00946595 | Evaluation of a Lopinavir/Ritonavir Monotherapy vs a Triple Therapy as Maintena… | Phase2 | HIV Infections | Completed | 2009-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01210807 | Clinical Evaluation of the One-Piece Tecnis Multifocal Intraocular Lens (IOL) | Phase4 | Cataract | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00977080 | Evaluation of the Effectiveness of Paricalcitol Versus Cinacalcet With Low-Dose… | Phase4 | Chronic Kidney Disease | Completed | 2009-11-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01074580 | Contrast Enhanced Ultrasonography (CEUS) of Patients With Crohn's Disease | — | Crohn's Disease | Terminated | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01071070 | Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyro… | Phase3 | Chronic Kidney Disease | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00799617 | The Testosterone Trials in Older Men | Phase3 | Andropause | Completed | 2009-11-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01043458 | Pharmacokinetic Study of ABT-126 in Stable Subjects With Schizophrenia | Phase1 | Schizophrenia | Completed | 2009-11-01 | — | ClinicalTrials.gov |
| NCT01025492 | Study of Trilipix Effects on Lipids and Arteries | Phase4 | Dyslipidemia | Terminated | 2009-11-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01006629 | Palivizumab for Prevention of Severe Respiratory Syncytial Virus Infection in R… | Phase2 | Respiratory Syncytial Virus Infection | Completed | 2009-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01009788 | ABT-888 and Temozolomide for Metastatic Breast Cancer and BRCA1/2 Breast Cancer | Phase2 | Breast Cancer | Completed | 2009-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00933153 | Effectiveness of Oral Nutritional Supplements (ONS) in a Meals-on-Wheels Popula… | Na | Elderly | Completed | 2009-10-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00984204 | Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the … | Phase3 | Typical Atrial Flutter | Completed | 2009-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00987610 | Guidewire for Chronic Total Occlusion | Phase4 | Coronary Occlusion | Completed | 2009-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00990704 | Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With S… | Phase2 | Secondary Hyperparathyroidism | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01003275 | Metabolic Effects of Paricalcitol | Phase2 | Chronic Kidney Disease | Completed | 2009-10-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01009216 | A Study of ABT-384 Levels and Pharmacodynamic Activity Measured in Cerebrospina… | Phase1 | Healthy | Completed | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01418703 | Feasibility Study of a Modular Control to Range System in Type 1 Diabetes Melli… | Na | Type 1 Diabetes Mellitus | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01048970 | Effect on the Nutritional and Inflammatory Status of Docosahexaenoic Acid (DHA)… | Phase2 | Lung Cancer | Unknown | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01053520 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female … | Phase1 | Healthy Female Subjects | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01014741 | Modified Ablation Guided by Ibutilide Use in Chronic Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2009-10-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00972621 | Clinical Evaluation of a New Viscoelastic for Cataract Surgery | Na | Cataract | Completed | 2009-09-30 | 2010-11-30 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00872664 | Skin and Serum Carotenoids in Preterm Infants Fed on a Formula Supplemented Wit… | Na | Retinopathy of Prematurity | Completed | 2009-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00903838 | A Pilot Study to Assess Efficacy and Safety of Pardoprunox as Adjunct Therapy t… | Phase2 | Advanced Stage Parkinson's Disease | Terminated | 2009-09-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01792206 | Effect Of Paricalcitol (Zemplar) On Endothelial Function And Inflammation In Ty… | Na | Type 2 Diabetes | Unknown | 2009-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01058837 | SCD-HeFT 10 Year Follow-up | — | Left Ventricular Systolic Dysfunction | Unknown | 2009-09-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01051596 | A Study of ABT-888 in Combination With Temozolomide for Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00982826 | Single and Multiple Dose Evaluation of ABT-072 and to Evaluate the Effect of Fo… | Phase1 | Hepatitis C | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00977964 | Tolerance of Healthy Term Infants Fed Infant Formulas #3 | Phase3 | Gastrointestinal Tolerance | Completed | 2009-09-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00951795 | Accuracy of the Pima™ CD4 Test for Enumeration of CD4+ T-Cell Counts | — | HIV Infection | Withdrawn | 2009-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00931463 | A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Followi… | Phase4 | HIV Infections | Completed | 2009-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00933764 | Clinical Performance Evaluation of the Cholestech LDX Cardiac hsCRP Test (CLEAR) | — | Cardiovascular Disease | Withdrawn | 2009-08-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01348022 | Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary A… | — | Coronary Artery Disease | Completed | 2009-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01786486 | AMPLATZER Cardiac Plug (ACP) Registry-Long Term Follow-up Protocol | — | Atrial Fibrillation | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01106534 | XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort | Phase4 | Chronic Total Occlusion of Coronary Artery | Completed | 2009-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01217528 | Reduction of Inappropriate Implantable Cardioverter Defibrillator (ICD) Therapi… | Na | Cardiac Death | Completed | 2009-08-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01000675 | Registry for Study of Coils in Intracranial Aneurysms | — | Cerebral Aneurysms | Completed | 2009-08-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01037270 | Evaluation of the Accuracy and Precision of the INRatio® Prothrombin Time (PT) … | — | Pulmonary Embolism | Completed | 2009-08-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00968422 | A Study of Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ABT-… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00941746 | Safety and Tolerability of PG110 in Patients With Knee Osteoarthritis Pain | Phase1 | Osteoarthritis, Knee | Completed | 2009-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00964938 | Multisite Pacing With a Quadripolar Lead | Phase4 | Heart Failure | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959816 | A Study to Investigate the Process by Which ABT-614 is Absorbed, Distributed, M… | Phase1 | Healthy | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT00959634 | Pharmacokinetic Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2009-08-01 | — | ClinicalTrials.gov |
| NCT01095978 | Evaluation of the Treatment With Klacid SR in Patients With Acute Tracheitis, T… | — | Respiratory Tract Infections | Completed | 2009-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00946231 | Heart Failure (HF) Assessment With B-type Natriuretic Peptide (BNP) In The Home | — | Heart Failure | Completed | 2009-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00972218 | Effectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease | Phase4 | Spondyloarthritis | Withdrawn | 2009-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00974831 | Glucose Tolerance in Healthy Overweight Adults | Phase2 | Overweight | Completed | 2009-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00940862 | Effect of Adalimumab on Vascular Inflammation in Patients With Moderate to Seve… | Phase4 | Psoriasis | Completed | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00937573 | Xience V at Wake Forest University Baptist Medical Center (WFUBMC) | — | Percutaneous Coronary Intervention | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00949000 | AnalyST Treadmill Study | Na | Ischemic Heart Disease | Completed | 2009-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00947440 | Evaluation of the Bioavailability of Two ABT-072 Tablet Formulations as Compare… | Phase1 | Hepatitis C | Completed | 2009-07-01 | — | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00888108 | Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Com… | Phase1 | Solid Tumor | Completed | 2009-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00979979 | Clinical Performance of Abbott RealTime Hepatitis C Virus (HCV) Genotype II Test | — | Hepatitis C | Completed | 2009-07-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00735722 | A(f)MAZE-CABG Study | Na | Coronary Arteriosclerosis | Terminated | 2009-07-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00958451 | Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02485093 | To Pace or Not to Pace in Sinus Node Disease | Na | Sinus Node Disease | Completed | 2009-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00881842 | Annual Study to Investigate Inactivated Subunit Influenza Vaccine Due to New Vi… | Phase3 | Influenza | Completed | 2009-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01171950 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Withdrawn | 2009-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01305525 | A Prospective Clinical Outcomes Registry | — | Pain | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00940888 | SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac R… | — | Tachyarrhythmias | Completed | 2009-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01056744 | Optical Coherence Tomography to Evaluate Paclitaxel-Eluting Balloons and Everol… | Phase4 | Stents | Completed | 2009-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00912431 | Pharmacokinetic and Exploratory Biomarker Study of ABT-126 in Healthy Volunteers | Phase1 | Healthy | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00916370 | SPIRIT PRIME Clinical Trial | Phase3 | Myocardial Ischemia | Completed | 2009-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00919490 | A Study of Single Dose of ABT-333 in Healthy Male Adults | Phase1 | HCV Infections | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922571 | A Study of Cataract Surgery With the Femtosecond Laser | Na | Cataract | Terminated | 2009-06-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00925522 | Therapy Cool Path Ablate VT | Na | Ischemic Ventricular Tachycardia | Terminated | 2009-06-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00931281 | Study in Healthy Adults to Evaluate Pharmacokinetics, Safety and Tolerability o… | Phase1 | HCV Infection | Completed | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00933933 | Evaluation of Diagnostic HIV Ag/Ab Combo Assay | Phase3 | Human Immunodeficiency Viruses | Completed | 2009-06-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00909636 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Multiple As… | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00891813 | Effectiveness and Safety of IV Zemplar in Patients on Hemodialysis and With Sec… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00905853 | Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy | Phase4 | Recurrent Ventricular Tachycardia | Completed | 2009-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00909311 | Study in Healthy Adults to Evaluate Effect of Food on Pharmacokinetics, Safety … | Phase1 | HCV Infection | Completed | 2009-05-01 | — | ClinicalTrials.gov |
| NCT00889889 | Immunogenicity and Safety of a Cell-derived Influenza Vaccine in Adults Aged >=… | Phase2 | Influenza | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00867048 | Strategic Timing of Antiretroviral Treatment | Phase4 | HIV Infection | Completed | 2009-04-15 | 2022-07-27 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00735085 | A Phase 2a Dose Escalation Study With SLV334 in Patients With Traumatic Brain I… | Phase2 | Traumatic Brain Injury | Terminated | 2009-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00888667 | Optimal EGM Configuration for Morphology Discrimination | — | Premature Ventricular Complexes | Terminated | 2009-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00890318 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895102 | Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulati… | Phase1 | HCV Infection | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00895401 | DaVita Assessment of Nutritional Supplement Effects (DANSE) | Phase4 | Malnutrition | Completed | 2009-04-01 | — | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00519194 | CONcomitant eValuation of Epicor Left atRial Therapy for AF | Na | Atrial Fibrillation | Terminated | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00941447 | Development of Self-Regulation in Individuals With Type 2 Diabetes | Na | Type 2 Diabetes | Completed | 2009-04-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00918255 | Study of Adalimumab in Subjects With Moderate to Severe Chronic Hidradenitis Su… | Phase2 | Hidradenitis Suppurativa | Completed | 2009-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076166 | Recovery Time in Children With Lower Respiratory Tract Infections Treated With … | — | Lower Respiratory Tract Infection | Completed | 2009-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01024855 | Comparative Evaluation of Corneal Staining With Balafilcon A Lenses and Two Mul… | Phase1 | Myopia | Completed | 2009-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00907361 | The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MR… | — | Need for MRI Imaging With Pacemaker or | Completed | 2009-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00930839 | Role of Prostaglandins on Niacin-Induced Flushing | — | Flushing | Completed | 2009-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00854659 | A Safety, Tolerability and Pharmacokinetic Study of ABT-102 in Healthy Subjects | Phase1 | Healthy Volunteers | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00874445 | Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configurat… | — | Sudden Cardiac Death | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00870467 | A Study of Adalimumab in Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2009-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00867399 | A Safety and Tolerability Study of ABT-126 in Elderly | Phase1 | Alzheimer's Disease | Completed | 2009-03-01 | — | ClinicalTrials.gov |
| NCT00873691 | Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants | — | Healthy | Completed | 2009-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00870324 | OptiSense™ Performance in Detecting Atrial Episodes | — | Tachyarrhythmias | Completed | 2009-03-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00882219 | Clinical Evaluation of Patients With Everolimus-eluting Stent Xience V® Implant… | Phase3 | Coronary Restenosis | Completed | 2009-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00844532 | Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Ex… | Phase3 | Peripheral Vascular Disease | Completed | 2009-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00961051 | Evaluation of an Investigational Multi-Purpose Solution (MPS) | Phase3 | Study Focus is Healthy Contact Lens Wearers | Completed | 2009-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00845741 | Neutrophil Gelatinase-associated Lipocalin (NGAL) Evaluation in Emergency Depar… | — | Acute Kidney Injury | Completed | 2009-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00823303 | Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kid… | Phase4 | Secondary Hyperparathyroidism | Completed | 2009-02-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01097733 | Dual-Source Computed Tomography to Improve Prediction of Response to Cardiac Re… | — | Heart Failure - NYHA II - IV | Completed | 2009-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00913081 | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) | Phase4 | Flushing | Completed | 2009-02-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00839293 | Comparison of Fenofibric Acid Bioavailability From ABT-335 Capsules | Phase1 | Healthy | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01931956 | Real World Expanded Multicenter Study of the MitraClip® System (REALISM) | Na | Mitral Valve Insufficiency | Completed | 2009-01-22 | 2018-06-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00623025 | Creon in HIV Patients With Steatorrhea | Phase3 | Steatorrhea | Terminated | 2009-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00870948 | Phase 1 BA Study, Single Center With Healthy Volunteers | Phase1 | Healthy | Completed | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01704599 | Addition of Modulators of Homocysteine to Adalimumab Therapy in the Treatment o… | Phase1 | Psoriasis | Terminated | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00616902 | The PRIMO II Study: Paricalcitol Injection Benefits in Renal Failure Induced Ca… | Phase3 | Chronic Kidney Disease (CKD) Stage 5 | Terminated | 2009-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00809510 | A Study of the Long-term Safety of ABT-089 for Subjects With Mild-to-moderate A… | Phase2 | Alzheimer's Disease | Terminated | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01005927 | Fructooligosaccharide and Calcium Absorption in Adolescent Girls | Phase1 | Osteoporosis | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00664430 | Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism | Terminated | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00865007 | Lopinavir/r Monotherapy Versus Abacavir/Lamivudine and Lopinavir/r for Limb Fat… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01088516 | Clinical Study of an Aluvia-based HAART Regimen for Prevention of Mother-to-chi… | Phase4 | HIV | Completed | 2008-12-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01078584 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients | — | Hypertension | Completed | 2008-12-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00798382 | Comparative Gastrointestinal Tolerance of Various Infant Formulas in Healthy Te… | Phase2 | Infant, Newborn | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00832975 | AVAI: Atrial Ventricular Arrythmia Incidence | — | Ventricular Tachycardia | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00865475 | Prevention of Lipoatrophy in Patients Treated With Lopinavir/Ritonavir in Monot… | Phase4 | HIV Infection | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00788801 | Exploratory Positron Emission Tomography (PET) Study to Evaluate the Effects of… | Phase1 | Healthy Volunteers | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00807586 | Corticosteroid Pulse After Ablation | Phase4 | Atrial Fibrillation | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00874289 | Utility of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Predicting Rena… | — | Heart Failure | Completed | 2008-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076153 | Recovery Time in Thai Patients With Upper or Lower Respiratory Tract Infections… | — | Respiratory Tract Infection | Completed | 2008-12-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01772940 | Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a… | Phase4 | HIV-1 Infection | Completed | 2008-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00502372 | Effect of an Oral Supplement Enriched in Amino Acids and the Leucine Metabolite… | Phase1 | Pressure Ulcers | Terminated | 2008-12-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00811551 | Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices | — | Heart Failure | Completed | 2008-12-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00780156 | The ITALIC Study: Is There A LIfe for Drug-eluting Stents (DES) After Discontin… | — | Restenosis | Terminated | 2008-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT02198716 | Xience or Vision Stent Management of Angina in the Elderly | Na | Coronary Artery Disease | Completed | 2008-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT00771498 | An Evaluation of the Pharmacological Interaction of Lopinavir/r and Rifampin | Phase4 | HIV Infection | Completed | 2008-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01084668 | Quality of Life in Adalimumab Treated Psoriasis Patients Failing Other Biologic… | — | Psoriasis Chronic | Completed | 2008-11-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01154751 | Data Registry Following Patients Using Supera Stent in the Femoral Arteries | Na | Peripheral Artery Disease | Terminated | 2008-11-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00762320 | Comparison of Liquid Kaletra and Low Dose Kaletra Tablets | Na | HIV Infections | Completed | 2008-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00796679 | Oral Paricalcitol in Stage 3 - 5 Chronic Kidney Disease | Na | Chronic Kidney Disease | Completed | 2008-10-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00768690 | A Study in Healthy Adult Subjects to Evaluate the Safety, Tolerability, and Pha… | Phase1 | HCV Infection | Completed | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00731237 | XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Exc… | — | Atherosclerosis | Completed | 2008-10-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00798291 | Evaluation of AN777 in Elderly Subjects | Phase2 | Aged | Completed | 2008-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00775606 | Immune Reconstitution of Lopinavir/Ritonavir-Based vs Efavirenz-based HAART in … | Phase4 | Acquired Immune Deficiency Syndrome | Terminated | 2008-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01288976 | ACCESS-Europe A Two-Phase Observational Study of the MitraClip® System in Europe | — | Mitral Valve (MV) Regurgitation | Completed | 2008-10-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00819793 | CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulm… | Na | Heart Failure | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00832988 | CONFIRM - Comparison of in Office Interrogation Versus Remote Measurements | — | Pacemaker | Completed | 2008-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00783796 | SPIRIT Small Vessel Registry | Na | Coronary Artery Disease | Terminated | 2008-10-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01077271 | Compliance to Synagis (Palivizumab) Under Daily Pediatrician´s Conditions in Pr… | — | Premature Infants | Completed | 2008-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00814866 | Bone Resorption, Osteoclastogenesis and Adalimumab | Na | Rheumatoid Arthritis | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00693745 | Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type N… | — | Acute Decompensated Heart Failure | Completed | 2008-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00785616 | A Trial to Determine the Long-term Durability of Virologic Suppression in Kalet… | Phase4 | HIV Infection | Completed | 2008-09-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00683176 | Effect of Choline Fenofibrate (SLV348) on Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2008-09-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00754104 | Study of ABT-869 in Combination With Tarceva in Subjects With Solid Tumors | Phase1 | Solid Tumors | Withdrawn | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752687 | A Study of ABT-072 in Healthy and Hepatitis C Virus Genotype 1-Infected Adults | Phase1 | Hepatitis C | Completed | 2008-09-01 | — | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00752102 | Vitamin D and Coronary Calcification Study | Phase4 | Chronic Kidney Disease | Completed | 2008-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01223469 | TOCCATA - Touch+™ for Catheter Ablation | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00743522 | Programming Implantable Cardioverter Defibrillators in Patients With Primary Pr… | — | Shock | Completed | 2008-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01083693 | Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arth… | — | Rheumatoid Arthritis | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00747318 | A Phase 3, Multicenter, Open-label Continuation Study in Moderate to Severe Ast… | Phase3 | Asthma | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01078545 | Lucrin® Depot Efficacy and Safety Monitoring Study in Patients With Advanced Pr… | — | Advanced Prostate Cancer | Completed | 2008-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00752037 | Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients | Phase4 | HIV Infections | Completed | 2008-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00746564 | Study of New Implantable Loop Recorder | Na | Tachyarrhythmias | Completed | 2008-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00734292 | Single-dose Crossover Study to Evaluate the Early Bronchodilating Effect of Flu… | Phase2 | Mild to Moderate Asthma | Completed | 2008-09-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00752856 | Raltegravir + Lopinavir/Ritonavir Versus Efavirenz + Tenofovir + Emtricitabine … | Phase2 | HIV Infections | Completed | 2008-08-26 | 2014-02-11 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00743470 | A Bioavailability Study of Rifabutin and Lopinavir/Ritonavir in Healthy Adult S… | Phase1 | HIV | Terminated | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00753181 | Effects of Nutritional Products on Blood Glucose in Subjects With Type 2 Diabet… | Phase3 | Diabetes Mellitus, Type 2 | Completed | 2008-08-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00911703 | Determining When Patients Hospitalized With Acute Heart Failure Can Be Safely S… | — | Acute Heart Failure | Completed | 2008-08-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00713700 | AMPLATZER Duct Occluder II Clinical Study | Na | Patent Ductus Arteriosus | Completed | 2008-08-01 | 2016-10-05 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00746356 | Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds | Na | Heart Failure | Completed | 2008-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00735787 | Controlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Han… | Phase4 | Psoriasis | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00743028 | Assess the Oral Bioavailability of New ABT-263 Formulations | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2008-08-01 | — | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT00997828 | Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Cor… | Na | Coronary Artery Disease | Terminated | 2008-07-28 | 2019-04-05 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01120379 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Chronic Coronary Occlusion | Completed | 2008-07-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00817349 | Angio-Seal Evolution Device Registry | — | Peripheral Vascular Disease | Completed | 2008-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738764 | A Trial of PDL192 in Subjects With Advanced Solid Tumors | Phase1 | Cancer | Completed | 2008-07-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00711009 | Study Comparing Lopinavir/Ritonavir (LPV/r) + Emtricitabine/Tenofovir Disoproxi… | Phase3 | Human Immunodeficiency Virus Infection | Completed | 2008-07-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00701805 | Long-term Safety Study of Paricalcitol Injection in Chronic Kidney Disease Pati… | Phase2 | Secondary Hyperparathyroidism | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00676520 | XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIE… | — | Coronary Artery Disease | Completed | 2008-07-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00401076 | A Open-label Study to Assess the Safety of Oral Long-term Use of SA-001 in Panc… | Phase3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | Completed | 2008-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01027260 | Study to Evaluate the Role of Itopride HCI in Patients With Irritable Bowel Syn… | Phase2 | Irritable Bowel Syndrome | Completed | 2008-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00711217 | Evaluation of a Medical Food for Chronic Wounds | Phase3 | Foot Ulcer, Diabetic | Completed | 2008-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00700115 | Kaletra-isentress Treatment Evaluation | Phase4 | HIV Infections | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00705562 | Tolerance of Healthy Term Infants Fed Infant Formulas | Phase2 | Infant, Newborn | Completed | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00698607 | Efficacy of Xience/Promus Versus Cypher in rEducing Late Loss After stENTing | Phase4 | Coronary Artery Disease | Completed | 2008-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00694473 | Continuous Glucose Monitoring With a Subcutaneous Sensor During Critical Illnes… | Na | Critical Illness | Completed | 2008-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00842179 | Groin Complications Post Percutaneous Coronary Intervention Using Either Manual… | — | Vascular Closure | Completed | 2008-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00635817 | A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat C… | Phase3 | Puberty, Precocious | Completed | 2008-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00987506 | Evaluation of a XIENCE V® Endoprothesis Used for Coronary Angioplasty, for LPPR… | — | Coronary Artery Disease | Completed | 2008-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00631228 | XIENCE V® Everolimus Eluting Coronary Stent System India Post-marketing Single-… | — | Coronary Disease | Completed | 2008-06-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01076959 | Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid A… | — | Rheumatoid Arthritis | Completed | 2008-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00728910 | Combined Effects of Non-statin Treatments on Apolipoprotein A-I Up-Regulation (… | Phase2 | Dyslipidemia | Completed | 2008-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00577187 | Placement of CS/LV Pacing Leads With EnSite NavX Guidance | Early_Phase1 | Heart Failure | Withdrawn | 2008-06-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00727012 | Multicenter International Trial Ring AnnulopLasty | Na | Mitral Valve Insufficiency | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01350869 | Evaluation of Everolimus-Eluting Stents (The K-XIENCE Registry) | — | Coronary Artery Disease | Completed | 2008-06-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00690573 | Safety, Efficacy, and Pharmacokinetics of Adalimumab in Japanese Children With … | Phase3 | Juvenile Rheumatoid Arthritis | Completed | 2008-05-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00726869 | A Phase 1/2, Multi-center, Open-label, Dose-escalation Study of Elotuzumab(Huma… | Phase1 | Multiple Myeloma | Terminated | 2008-05-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00679926 | Kaletra and Viread in Antiretroviral Naïve Patients | Phase4 | HIV Infections | Terminated | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00657774 | A Phase I Study in Asthma Patients Evaluating the Effect of Doses of FlutiForm™… | Phase1 | Asthma | Completed | 2008-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00666237 | Primary Tube Versus Trabeculectomy Study | Phase4 | Glaucoma | Completed | 2008-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT00666692 | A Phase 1b Study With Volociximab in Combination With Carboplatin, Paclitaxel, … | Phase1 | Non-small Cell Lung Cancer | Completed | 2008-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00667576 | Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patient… | Phase2 | Chronic Kidney Disease on Hemodialysis | Completed | 2008-04-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00681525 | A Multiple-Dose Pharmacokinetic Interaction Study Between ABT-335, Atorvastatin… | Phase1 | Pharmacokinetics | Completed | 2008-04-01 | — | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01076218 | Navigator 1.5 Accuracy Study | — | Diabetes Mellitus | Completed | 2008-04-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01074931 | Clinical, Virological and Safety Outcomes of a Lopinavir/Ritonavir-Based Regime… | — | HIV-1 Infections | Completed | 2008-04-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01083160 | Clinical Outcomes, Compliance and Effectiveness of Switching From Infliximab or… | — | Rheumatoid Arthritis | Terminated | 2008-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00902005 | Endothelial Function, Inflammatory Disease Activity, and Bone and Cartilage Mar… | — | Rheumatoid Arthritis | Completed | 2008-04-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00960648 | Registry to Evaluate Efficacy of Xience/Promus Versus Cypher in Reducing Late L… | — | Coronary Artery Disease | Completed | 2008-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01103596 | Evaluation of the Public Health Interest of Kaletra: Impact on Resistance to An… | — | HIV Infection | Completed | 2008-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01244308 | Effectiveness and Reliability of VectSelect™ Feature for Avoidance of Phrenic N… | — | Heart Failure | Completed | 2008-03-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00647387 | Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscul… | Na | Ventricular Septal Defects | Completed | 2008-03-01 | 2024-02-23 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00693329 | Neutrophil Gelatinase-associated Lipcalin(NGAL): A Novel Blood Marker for Deter… | — | Cardiovascular Surgery With Coronary Angiography | Completed | 2008-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00617162 | Deep Brain Stimulation for Major Depressive Disorder | Na | Depressive Disorder, Major | Terminated | 2008-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00649025 | A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combina… | Phase3 | Asthma | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00574431 | ICU Nutrition Study Bern | Phase4 | Critical Illness | Completed | 2008-02-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00630877 | Evaluation of a Flushing ASsessment Tool (FAST) in Subjects Receiving Niacin Ex… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00626431 | A Study of Leuprolide to Treat Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2008-02-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00639158 | Safety and Efficacy Study Comparing ABT-335 Coadministered With Atorvastatin an… | Phase3 | Dyslipidemias | Completed | 2008-02-01 | — | ClinicalTrials.gov |
| NCT00626392 | Study to Evaluate the EFFECTS of Acetylsalicylic Acid (ASA) on Niaspan®-Induced… | Phase3 | Dyslipidemia | Completed | 2008-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00561093 | Anit-Inflammatory and Anti-Oxidative Nutrition in Dialysis Patients | Phase3 | Hypoalbuminemia | Completed | 2008-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00667355 | A Study of Adalimumab in Japanese Subjects With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00726440 | Are the Continuous Glucose Monitoring Systems Able to Improve Long Term Glycaem… | Na | Type 1 Diabetes | Completed | 2008-02-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00606463 | Gen2 Isthmus-Dependent Atrial Flutter Ablation Study | Na | Atrial Flutter | Terminated | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00866021 | Treatment of HIV/HCV Coinfection With Peg-IFN and Ribavirin in Patients Receivi… | Phase4 | HIV/HCV Co-infection | Completed | 2008-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00632372 | Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study | — | Heart Failure | Completed | 2008-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00626093 | 'Effect of CRT on Defibrillation Threshold Estimates' Study | Phase4 | Sudden Cardiac Death | Completed | 2008-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00818077 | Using Continuous Glucose Monitoring to Understand the Glycemic Impact of Food | — | Type 2 Diabetes | Completed | 2008-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00585481 | Incidence of Severe Respiratory Syncytial Virus Infections in Preterm Brazilian… | — | Respiratory Syncytial Viruses | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00738725 | BioImage Study: A Clinical Study of Burden of Atherosclerotic Disease in an At-… | — | Plaque | Completed | 2008-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01230606 | Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Inte… | — | Cardiovascular Disease | Completed | 2008-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00597623 | Efficacy Study of an Anti-Tumor Necrosis Factor (TNF) Alpha Agent in Patients W… | Phase3 | Hand Osteoarthritis | Completed | 2008-01-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01163916 | Study to Characterize Demographics, Compliance, Tolerability and Safety in Pati… | — | Rheumatoid Arthritis | Completed | 2008-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00566722 | Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to S… | Phase3 | Psoriasis | Completed | 2008-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00652522 | Atrial Fibrillation Management in Congestive Heart Failure With Ablation | Na | Persistent Atrial Fibrillation | Completed | 2008-01-01 | 2017-07-13 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01231321 | A Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy … | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01143818 | ESPRIT Study in Hypogonadal Men | — | Hypogonadism | Completed | 2007-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00559559 | PAtient NOtifier Feature for Reduction of Anxiety | Na | Tachycardia, Ventricular | Completed | 2007-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00919165 | Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Pl… | — | Cognitive Function in Carotid Stenting | Completed | 2007-12-01 | 2017-04-20 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00647270 | Study Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inf… | Phase3 | Rheumatoid Arthritis | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00632450 | EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study | — | Heart Failure | Completed | 2007-12-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00609245 | Effect of Valproic Acid Concentration on Photic Response | Phase4 | Photosensitive Epilepsy | Completed | 2007-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00562887 | Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intra… | Phase2 | Crohn's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00727181 | An Observational, Prospective Evaluation of the Trifecta™ Valve | Na | Aortic Valve Insufficiency | Completed | 2007-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00574249 | Adalimumab in Combination With Topical Treatment (Calcipotriol/Betamethasone) i… | Phase3 | Chronic Plaque Psoriasis | Completed | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01078116 | Cost Utility Analyses of Adalimumab Treatment in Patients With Rheumatoid Arthr… | — | Rheumatoid Arthritis | Completed | 2007-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00819117 | Investigation of Transvenous Versus Epicardial Left Ventricular Stimulation Tec… | Na | Heart Failure | Completed | 2007-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT01754064 | St. Jude Medical Product Longevity and Performance (SCORE) Registry | — | Bradycardia | Completed | 2007-11-01 | 2020-07-10 | ClinicalTrials.gov |
| NCT00631774 | A Study to Evaluate the Postprandial Metabolic Response After Use of Glucerna S… | Na | Type 2 Diabetes | Completed | 2007-11-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00746135 | TRI-V Heart Failure (HF) Implanted Cardioverter Defibrillator (ICD) Study | Na | Heart Failure | Completed | 2007-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00970567 | Ketoacidosis in Individuals With Type I Diabetes Mellitus (T1DM) | Na | Type 1 Diabetes | Completed | 2007-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00554385 | A Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/H… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00555204 | Safety and Efficacy Study of ABT-089 in Adults With Mild to Moderate Alzheimer'… | Phase2 | Alzheimer's Disease | Terminated | 2007-11-01 | — | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00544206 | Comparison of Enteral Products for Tube Fed Patients With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-10-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01079195 | Effectiveness and Tolerability of Tarka® in the Treatment of Hypertensive Patie… | — | Hypertension | Completed | 2007-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00660647 | Optimized Treatment Algorithm for Patients With Early Rheumatoid Arthritis (RA) | Phase3 | Arthritis, Rheumatoid | Completed | 2007-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01084538 | Study of Zemplar iv in Patients With End Stage Chronic Kidney Disease, Undergoi… | — | Parathyroid Hormone | Completed | 2007-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01107535 | Effectiveness of Synagis (Palivizumab) Immunoprophylaxis in Preterm Infants Wit… | — | Respiratory Syncytial Virus Infection | Completed | 2007-09-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00537979 | Efficacy and Safety of 6 Months Treatment With Paricalcitol Injection or Oral i… | Phase4 | Secondary Hyperparathyroidism | Completed | 2007-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00918294 | QuickOptTM Study - Using the QuickOptTM Method for Timing Cycle Optimization | Na | Heart Failure | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00513370 | A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inade… | Phase3 | Psoriasis | Completed | 2007-09-01 | — | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01310309 | EXecutive Registry: Evaluating XIENCE V® in a Multi Vessel Disease | — | Coronary Disease | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00543673 | Tolerance of Healthy, Term Infants to Infant Formulas | Phase2 | Healthy | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00686205 | Evaluation of a Human Immunodeficiency Virus (HIV) Blood Screening Assay | Phase3 | Healthy Donors | Completed | 2007-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00650936 | Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Appr… | Na | Atrial Septal Defect | Completed | 2007-08-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00538902 | Safety and Efficacy Study of Adalimumab in Adult Chinese Rheumatoid Arthritis S… | Phase2 | Rheumatoid Arthritis | Completed | 2007-08-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00520065 | Comparison of Nutritional Products for People With Type 2 Diabetes | Phase2 | Type 2 Diabetes Mellitus | Completed | 2007-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00512863 | A Dose-Finding Study to Evaluate the Safety, Efficacy and Pharmacokinetics of A… | Phase2 | Asthma | Withdrawn | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00490841 | The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Re… | Na | Renal Artery Obstruction | Completed | 2007-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01114269 | PRE-DETERMINE Cohort Study | — | Coronary Artery Disease | Active_Not_Recruiting | 2007-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT00496938 | XIENCE V: SPIRIT WOMEN | Phase4 | Coronary Artery Stenosis | Completed | 2007-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00481013 | Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2007-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00558857 | Dynamic Substrate Mapping (DSM) for Ischemic VT | Phase1 | Ischemic Ventricular Tachycardia | Terminated | 2007-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00491530 | A Year 2, Safety Extension Study of the Combination of ABT-335 and Statin Thera… | Phase3 | Mixed Dyslipidemia | Completed | 2007-06-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00489177 | Optimal Programming to Improve Mechanical Indices, Symptoms and Exercise in Car… | Phase4 | Heart Failure | Completed | 2007-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00487279 | DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation | Na | Coronary Artery Disease | Terminated | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00473356 | Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bar… | Na | Obesity | Completed | 2007-06-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00473148 | B-type Natriuretic Peptide for the Management of Weaning | Phase3 | Respiratory Insufficiency | Completed | 2007-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00838175 | Characteristics Predictive of Success and Complications in the Use of Suture-Me… | — | Cardiac Catheterization | Unknown | 2007-06-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00475709 | Aortic Valve Replacement With Trifecta(TM) | Na | Aortic Valve Insufficiency | Completed | 2007-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00329680 | The Effects of Eicosapentaenoic Acid (EPA), Gamma-Linolenic Acid (GLA) and Anti… | Phase4 | Sepsis | Completed | 2007-06-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00834457 | A Pilot Study Of the Effects of Highly Active Antiretroviral Therapy on Kaposi'… | Phase2 | AIDS-related Kaposi's Sarcoma | Completed | 2007-06-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00508222 | Kaletra Monotherapy in HIV/HCV Co-infected Subjects | Phase3 | HIV Infections | Completed | 2007-06-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00377871 | Hemodynamic Performance in Stentless Heart Valves | Na | Heart Valve Diseases | Completed | 2007-05-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00469638 | Efficacy and Safety Study on Agilis NxT Introducer in AF Patients | Na | Atrial Fibrillation | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00475566 | A Safety and Efficacy Study of the Dynalink®-E Everolimus Eluting Peripheral St… | Na | Atherosclerosis | Completed | 2007-05-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00400842 | A Study of SA-001 to Treat Pancreatic Exocrine Insufficiency | Phase3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00465088 | An Open-Label Study to Compare the Lipid Effects of Niacin ER and Simvastatin (… | Phase3 | Hyperlipidemia | Completed | 2007-04-01 | — | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00636987 | Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra | Na | Aortic Valve Insufficiency | Completed | 2007-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00614458 | MK-0518 Intensification And HDAC Inhibition In Depletion Of Resting CD4+ T Cell… | Phase2 | HIV Infections | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00444379 | Anti-Retrovirals for Kaposi's Sarcoma | Phase4 | Kaposi's Sarcoma | Completed | 2007-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00409682 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Crohn's Disease | Completed | 2007-04-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00420355 | Pharmacokinetic Study of Two HIV Protease Inhibitors in Patients | Phase4 | HIV Infection | Terminated | 2007-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01615835 | EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant | Na | Congestive Heart Failure | Completed | 2007-04-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01634464 | Role of Nutrition and Maternal Genetics on the Programming of Development of Fe… | — | Obesity | Unknown | 2007-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00927069 | Safety and Efficacy of Adalimumab in Patients Who Showed an Unsatisfactory Resp… | Phase3 | Plaque Psoriasis | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00445432 | A Study of Adalimumab for the Maintenance of Clinical Remission in Japanese Sub… | Phase2 | Crohn's Disease | Completed | 2007-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00424814 | Prevention of HIV1 Mother to Child Transmission Without Nucleoside Analogue Rev… | Phase2 | HIV Infections | Completed | 2007-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00433199 | Testosterone Treatment for Hypogonadal Men | Phase3 | Hypogonadism | Completed | 2007-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00437476 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT01940120 | EVEREST II Pivotal Study High Risk Registry (HRR) | Na | Mitral Valve Insufficiency | Completed | 2007-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00827996 | To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Se… | Phase2 | Hidradenitis Suppurativa | Completed | 2007-02-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00437684 | Lopinavir/Ritonavir Monotherapy Versus Standard Highly Active Antiretroviral Th… | Phase3 | HIV Infections | Unknown | 2007-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445939 | A Study of Adalimumab for the Induction of Clinical Remission in Japanese Subje… | Phase2 | Crohn's Disease | Completed | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00354562 | A Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non… | Phase1 | Lung Cancer | Terminated | 2007-02-01 | — | ClinicalTrials.gov |
| NCT00445809 | Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Ev… | — | Kidney Failure, Acute | Completed | 2007-02-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00607776 | Artificial Tears Study in Mild to Moderate Dry Eye Patients | Phase2 | Dry Eye | Completed | 2007-01-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00587158 | Oral Paricalcitol in Kidney Transplant Recipients | Na | Transplant; Failure, Kidney | Completed | 2007-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00571961 | Pharmacokinetic Interactions Between Buprenorphine and Kaletra (Lopinavir/Riton… | Na | HIV Infections | Completed | 2007-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01343758 | Study Investigating the Use of Intravenous Fluids With Dextrose for Dehydrated … | Na | Gastroenteritis | Completed | 2007-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00429468 | A Study to Evaluate the Interaction Between Vicodin® CR and Ethanol in Healthy … | Phase1 | Drug Interactions | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00429091 | A Dose-Ranging Study of the Efficacy of ABT-894 in Adults With Attention-Defici… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2007-01-01 | — | ClinicalTrials.gov |
| NCT00427921 | Human Anti-TNF Monoclonal Antibody Adalimumab in Canadian Subjects With Moderat… | Phase3 | Crohn's Disease | Completed | 2007-01-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00413244 | The Cardiac Benefit of Testosterone Replacement in Men With Low Testosterone Le… | Phase3 | Coronary Artery Disease | Completed | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00402792 | A Study of Extended-Release Hydrocodone/Acetaminophen (Vicodin CR®) in Subjects… | Phase3 | Pain | Completed | 2006-12-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00369395 | A Study of Volociximab in Metastatic Melanoma | Phase2 | Stage IV Melanoma | Terminated | 2006-12-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT01075126 | Safety Study of Depakote Versus Lithium in African Americans With Bipolar Disor… | Phase4 | Bipolar Disorder | Withdrawn | 2006-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00747227 | Safety and Efficacy of a Violet Visible Light Blocking Intraocular Lens (IOL) | Phase3 | Cataract | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00397020 | Naturalistic Study, Comparison of Divalproex Extended Release (ER) and Quetiapi… | Phase4 | Bipolar Disorder | Completed | 2006-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00786708 | Sensitivity and Specificity of NGAL in an Emergency Room Population | — | Azotemia | Completed | 2006-12-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01081665 | Follow-up Patients With End Stage Renal Disease Receiving Zemplar to Prevent an… | — | Chronic Kidney Failure | Completed | 2006-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00415948 | Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Corona… | — | Acute Coronary Syndrome (ACS) | Completed | 2006-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00420927 | Study of the Optimal Protocol for Methotrexate and Adalimumab Combination Thera… | Phase4 | Rheumatoid Arthritis | Completed | 2006-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00412620 | An Evaluation of the Safety and Efficacy of ABT-925 in Subjects With Acute Exac… | Phase2 | Schizophrenia | Terminated | 2006-12-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00409617 | Study of Adalimumab Treatment for Induction and Maintenance of Clinical Remissi… | Phase3 | Crohn's Disease | Completed | 2006-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00421733 | The Effect of Paricalcitol Capsules on Reducing Albuminuria in Patients With Ty… | Phase2 | Diabetic Nephropathy | Completed | 2006-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00428246 | Study of Protective Effects of Paricalcitol on Inner Layer of Vessels and Its P… | Na | Chronic Kidney Disease | Completed | 2006-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00402740 | Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarter… | Na | Carotid Artery Disease | Completed | 2006-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00408629 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Activ… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00385736 | Efficacy and Safety of Adalimumab in Subjects With Moderately to Severely Acute… | Phase3 | Ulcerative Colitis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00347152 | Comparison of Immediate vs Gradual Switch to Divalproex in Adults With Intellec… | Na | Epilepsy | Completed | 2006-11-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00397657 | Comparative Study of the Effect of Ezetimibe Versus Extended-Release Niacin on … | Phase4 | Atherosclerosis | Terminated | 2006-11-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00761514 | Evaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheu… | Phase4 | Rheumatoid Arthritis | Terminated | 2006-11-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00402272 | SPIRIT V: Post-marketing Evaluation of the XIENCE V® Everolimus Eluting Coronar… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01171820 | SPIRIT V: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary St… | Phase4 | Coronary Disease | Completed | 2006-11-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00391729 | A Dose-Ranging, Cross-over Study of the Safety and Efficacy of ABT-089 in Adult… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2006-10-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00837798 | RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) … | — | Atrial Fibrillation | Completed | 2006-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00375557 | Safety and Efficacy of Divalproex and Quetiapine in Elderly Alzheimer's Dementi… | Phase4 | Alzheimer's Disease | Withdrawn | 2006-10-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00418314 | FREEDOM - A Frequent Optimization Study Using the QuickOpt Method | Na | Cardiac Arrhythmias | Completed | 2006-10-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00300430 | Study to Evaluate the Long-Term Safety and Efficacy of ABT-335, in Combination … | Phase3 | Dyslipidemia | Completed | 2006-09-01 | — | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00578617 | Ablation vs Drug Therapy for Atrial Fibrillation - Pilot Trial | Na | Atrial Fibrillation | Completed | 2006-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00274352 | A Study of Adalimumab to Treat Sarcoidosis of the Skin | Phase2 | Sarcoidosis | Completed | 2006-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00358917 | Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Ad… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2006-08-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00366158 | EVITA: Evaluation of VIP Feature in Pacemaker Patients | Na | Arrhythmia | Completed | 2006-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00367757 | STAR-AF:Substrate Versus Trigger Ablation for Reduction of Atrial Fibrillation … | Na | Atrial Fibrillation | Completed | 2006-08-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00380094 | Triage Now: an Observational, Prospective Multimarker Study of Biomarkers in Pa… | — | Acute Coronary Syndrome | Completed | 2006-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00307047 | SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluti… | Phase3 | Coronary Artery Disease | Completed | 2006-08-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01722188 | Lead Registry for Optim Leads | — | Optim Lead Insulation Related Adverse Events | Completed | 2006-08-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT00311181 | POWER (Pulse Width Optimized Waveform Evaluation Trial) | Phase4 | Sudden Cardiac Death | Completed | 2006-08-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01585064 | Optimization of Treatment With Adalimumab (Humira) | — | Rheumatoid Arthritis (RA) | Completed | 2006-08-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00417365 | Efficacy of (WaterWorks®)Douching Device for Elimination of Perceived Vaginal O… | Na | Vaginal Odor | Unknown | 2006-08-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00348153 | Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial) | Phase2 | Uveitis | Unknown | 2006-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00348283 | Effects of Adalimumab on Mucosal Healing in Subjects With Crohn's Disease Invol… | Phase3 | Crohn's Disease | Completed | 2006-08-01 | — | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00499148 | Efficacy Study Testing Herbal Extract on Metabolic Parameters in Subjects With … | Phase2 | Type 2 Diabetes | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01075178 | Retrospective Palivizumab Study in Children With Hemodynamically Significant Co… | — | Severe Respiratory Syncytial Virus Infection | Completed | 2006-07-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00356018 | Compliance With Once-Daily Divalproex Extended-Release Tablets (Depakote-ER) Ve… | — | Epilepsy | Completed | 2006-07-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00338650 | Treatment of the Human Anti-TNF Monoclonal Antibody Adalimumab in Moderate to S… | Phase3 | Crohn's Disease | Completed | 2006-06-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00334347 | A Comparison Study of the Efficacy and Tolerability of Depakote ER and Depakote… | Phase4 | Mania | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00432783 | A Comparison of Adherence Rates to Ritonavir and Its Accompanying Protease Inhi… | — | HIV Infections | Completed | 2006-06-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00414284 | BOOST: Study of Increased Dosage of Lopinavir/Ritonavir (LPV/r) | Phase4 | HIV Infections | Terminated | 2006-06-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00257920 | A Study of Zemplar® Injection and Hectorol® Injection on Intestinal Absorption … | Phase4 | Chronic Kidney Disease, Stage 5 | Completed | 2006-06-01 | — | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00439296 | ABT-751 With Chemotherapy for Relapsed Pediatric ALL | Phase1 | Recurrent Pediatric ALL | Terminated | 2006-05-22 | 2009-09-23 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00505570 | PRIMA PFO Migraine Trial | Phase2 | Migraine | Terminated | 2006-05-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00305539 | HECTHOR: Humira to Spare Steroids in Giant Cell Arteritis | Phase3 | Giant Cell Arteritis | Completed | 2006-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT01078571 | Safety and Effectiveness of Adalimumab in Patients Diagnosed With Rheumatoid Ar… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00328081 | State of Obesity Care in Canada Evaluation Registry | — | Obesity | Terminated | 2006-05-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00325949 | A Study of Pain Relief in Low Back Pain | Phase3 | Chronic Low Back Pain | Completed | 2006-05-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00315900 | Depakote Extended Release (ER) Versus Seroquel for Agitated Behaviors in Nursin… | Phase3 | Agitation | Terminated | 2006-05-01 | 2008-02-28 | ClinicalTrials.gov |
| NCT00427362 | A Canadian Open-Label Study to Evaluate the Safety and Effectiveness of Adalimu… | Phase3 | Psoriatic Arthritis | Completed | 2006-05-01 | — | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00318929 | Tolerability and Efficacy of Depakote-extended Release in the Elderly | Na | Elderly | Completed | 2006-04-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00467675 | Establishing Ambulatory Glucose Profiles for People Without Diabetes Using CGM … | — | NonDiabetes | Completed | 2006-04-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00307827 | Study of Visilizumab in Subjects With Intravenous Steroid-Refractory Ulcerative… | Phase2 | Ulcerative Colitis | Terminated | 2006-04-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00647400 | Adalimumab in Adult Japanese Subjects With Psoriasis | Phase2 | Psoriasis | Completed | 2006-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00311246 | Trial of Adalimumab in Progressive Sarcoidosis | Phase2 | Sarcoidosis | Terminated | 2006-04-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00312676 | Compare Tolerability of an Overnight Switch to Gradual Switch Between Two Diffe… | Phase4 | Epilepsy | Unknown | 2006-03-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00306475 | Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (AP… | Phase4 | Schizophrenia | Completed | 2006-03-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00300456 | Evaluate Safety and Efficacy of ABT-335 in Combination With Simvastatin in Subj… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300469 | Evaluate Safety and Efficacy of ABT-335 in Combination With Atorvastatin in Sub… | Phase3 | Mixed Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00603993 | Self-injection of Adalimumab in Adult Japanese Subjects With Rheumatoid Arthrit… | Phase3 | Rheumatoid Arthritis | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00294866 | Effect of Paricalcitol on Markers of Inflammation in Hemodialysis Patients | Phase4 | Kidney Failure | Completed | 2006-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00300131 | ABSORB Clinical Investigation, Cohort A (ABSORB A) Everolimus Eluting Coronary … | — | Coronary Disease | Completed | 2006-03-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00300482 | Evaluate Safety and Efficacy of ABT-335 in Combination With Rosuvastatin Calciu… | Phase3 | Dyslipidemia | Completed | 2006-03-01 | — | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00281606 | A Multicenter Study to Assess the Tolerability of Once Daily Lopinavir/Ritonavi… | Phase4 | HIV Infection | Completed | 2006-02-14 | 2012-06-13 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00311168 | Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic P… | Na | Bradycardia | Completed | 2006-02-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00298974 | A Study of Pain Relief in Osteoarthritis | Phase3 | Osteoarthritis | Completed | 2006-02-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00287053 | Effects of Divalproex Sodium on Food Intake, Energy Expenditure, and Posture Al… | Phase4 | Healthy | Completed | 2006-02-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00275262 | A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Foll… | Phase2 | Hodgkin Disease | Terminated | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00286585 | TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality | Phase4 | Coronary Artery Disease | Completed | 2006-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00478660 | An Open-Label Study to Evaluate the Response to Adalimumab in Patients With Act… | Phase3 | Ankylosing Spondylitis | Completed | 2006-02-01 | — | ClinicalTrials.gov |
| NCT00477893 | Danish Multicenter Study of Adalimumab in Spondyloarthritis | Phase4 | Spondyloarthritis | Unknown | 2006-02-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00355056 | PREMIUM Migraine Trial | Na | Migraine Headaches | Completed | 2006-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00560040 | Myocardial Injury is Not Related to Training Levels Among Recreational Particip… | — | Troponin | Completed | 2006-01-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00256165 | REST Study: Left Ventricular Regression European Study | Phase4 | Aortic Valve Stenosis | Completed | 2006-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00416013 | Correlations Between BNP & Dry Weight, and Between Troponin & Mortality, in Hem… | — | Kidney Failure, Chronic | Unknown | 2005-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00262522 | Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Ve… | Phase3 | Human Immunodeficiency Virus Infections | Completed | 2005-11-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00276432 | Diagnosis and Treatment of Acute Coronary Syndrome in the ED & the Impact of Ra… | Phase4 | Unstable Angina | Completed | 2005-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00404222 | A Study Comparing Vicodin® CR and NORCO® to Placebo in Subjects With Acute Pain… | Phase2 | Pain | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00338754 | Adalimumab in Adult Japanese Subjects With Moderate to Severe Chronic Plaque Ps… | Phase2 | Psoriasis | Completed | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00453622 | RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriur… | — | Heart Failure | Completed | 2005-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00126308 | Facial Lipoatrophy Trial: Immediate Versus Deferred Injections of Poly-L-Lactic… | Phase4 | HIV-Associated Lipodystrophy | Terminated | 2005-11-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00920881 | Clinical Evaluation of the Accuracy of the FreeStyle Navigator Continuous Gluco… | — | Diabetes Mellitus | Completed | 2005-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00287508 | Emboshield® and Xact® Post Approval Carotid Stent Trial (The EXACT Study) | Phase4 | Carotid Artery Disease | Completed | 2005-11-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT02087046 | Deep Brain Stimulation (DBS) for the Suppression of Tremor | Na | Tremor | Completed | 2005-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00783380 | Influenza Vaccination in Immunocompromized Patients | Phase4 | Immunosuppression | Completed | 2005-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00247143 | High Dose Ritonavir/Lopinavir Liquid Formulation in Salvage Therapy for Proteas… | Na | HIV | Unknown | 2005-10-01 | — | ClinicalTrials.gov |
| NCT00140751 | Comparison of Treatment Simplification by LPV/r vs Current Treatment Continuati… | Phase3 | HIV Infections | Completed | 2005-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00552474 | Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease | Na | Parkinson Disease | Completed | 2005-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT00885664 | Immune Reconstitution as a Determinant of Adverse Effects to New Antiretroviral… | Phase4 | HIV Infections | Completed | 2005-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00420966 | Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody T… | — | Lower Respiratory Tract Infection | Completed | 2005-10-01 | 2017-06-26 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00227266 | Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy | Phase2 | Spinal Muscular Atrophy | Completed | 2005-09-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00120289 | Niacin Plus Statin to Prevent Vascular Events | Phase3 | Cardiovascular Diseases | Terminated | 2005-09-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00573313 | Effects of SAMe in Patients With Alcoholic Liver Disease | Phase3 | Liver Disease, Alcoholic | Completed | 2005-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00586092 | A Phase I Study of ABT-510 in Combination With Bevacizumab in Advanced Solid Tu… | Phase1 | Solid Tumors | Completed | 2005-09-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00400231 | The Fenofibrate and Metformin for Atherogenic Dyslipidemia (FAMA) Study | Phase2 | Metabolic Syndrome x | Completed | 2005-08-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00209274 | Pivotal Study of a Percutaneous Mitral Valve Repair System | Na | Mitral Valve Insufficiency | Completed | 2005-08-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00235820 | Safety and Efficacy of Adalimumab to Methotrexate and Placebo in Subjects With … | Phase3 | Psoriasis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00790140 | Trial of Enteral Nutrition Enriched With Eicosapentaenoic Acid (EPA) in Upper G… | Phase4 | Esophageal Cancer | Unknown | 2005-07-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00211250 | Comparing Compliance, Tolerability, Efficacy and Adverse Events in Bipolar Tien… | Phase4 | Mood Disorder | Completed | 2005-07-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00235885 | Safety and Efficacy Study of Adalimumab in Patients With Active Psoriatic Arthr… | Phase3 | Psoriatic Arthritis | Completed | 2005-07-01 | — | ClinicalTrials.gov |
| NCT00180310 | SPIRIT II: A Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary S… | Phase3 | Coronary Disease | Completed | 2005-07-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00187239 | Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillato… | Phase4 | Arrhythmia | Completed | 2005-07-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00236002 | Cancer and Osteoporosis Research With Alendronate and Lupron (C.O.R.A.L ) | Phase3 | Osteoporosis | Terminated | 2005-07-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00195728 | Long Term Safety and Tolerability Study in Approximately 350 Subjects With Mode… | Phase3 | Moderate to Severe Chronic, Non-malignant Pain | Completed | 2005-06-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00148759 | Kaletra Sex/Gender Pharmacokinetics (PK) Study | Phase4 | HIV Infections | Completed | 2005-06-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00233558 | Open-Label Steroid Reduction Study of Adalimumab With Methotrexate in Patients … | Phase4 | Rheumatoid Arthritis | Terminated | 2005-06-01 | — | ClinicalTrials.gov |
| NCT00398333 | Study to Assess the Effectiveness of a Omega-3 Enriched Supplement on Chemother… | Phase4 | Colorectal Neoplasms | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00140101 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2005-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00543621 | An Intervention Program to Control Diabetes | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00166127 | Study of Blood Concentrations and Physiologic Effects of Levosimendan Given Dur… | Phase3 | Heart Failure | Terminated | 2005-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00419640 | SAFE Study - Septal Pacing for Atrial Fibrillation Suppression Evaluation | Na | Atrial Fibrillation | Completed | 2005-05-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00835822 | Efficacy and Safety of the Use of Venocur Triplex® in Patients With Chronic Ven… | Phase4 | Venous Insufficiency | Completed | 2005-05-01 | — | ClinicalTrials.gov |
| NCT00707837 | Nutritional Study in Preterm Infants | Phase3 | Preterm Infants | Completed | 2005-05-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01270087 | The Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthr… | Phase4 | Rheumatoid Arthritis | Completed | 2005-05-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00206830 | SHORTness of Breath In the Emergency Department (SHORTIE) | Phase2 | Acute Myocardial Infarction | Completed | 2005-04-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00109512 | Endometriosis Trial: Study of NBI-56418 in Endometriosis | Phase2 | Endometriosis | Completed | 2005-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00106938 | Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects… | Na | Carotid Artery Disease | Terminated | 2005-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00113334 | Study of ABT-510 (Thrombospondin Analogue) in Patients With Advanced Head and N… | Phase1 | Head and Neck Cancer | Completed | 2005-04-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00159224 | Induction-maintenance of Lopinavir/r in HIV-infected Subjects | Phase4 | HIV Infections | Completed | 2005-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00235105 | D2E7-Early AS | Phase2 | Ankylosing Spondylitis | Unknown | 2005-03-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00180505 | ASSESS Study: Evaluation of ABSOLUTE™ Stent System for Occluded Arteries | Phase4 | Peripheral Vascular Diseases | Completed | 2005-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00121472 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardi… | Na | Heart Failure, Congestive | Completed | 2005-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00234949 | A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderat… | Phase4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | Completed | 2005-03-01 | — | ClinicalTrials.gov |
| NCT00135226 | ASCEND: A Study of Cardiovascular Events iN Diabetes | Phase4 | Diabetes Mellitus | Active_Not_Recruiting | 2005-03-01 | 2037-07-31 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00547729 | Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOME… | Na | Heart Failure | Completed | 2005-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00195806 | Study Designed to Evaluate the Safety of Prophylactic Depakote ER in the Treatm… | Phase3 | Migraine | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00121485 | Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination The… | Na | Heart Failure, Congestive | Completed | 2005-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00160953 | Endorectal Coil Magnetic Resonance Images (ERC-MRI) | Phase2 | Prostatic Neoplasms | Completed | 2005-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00102713 | A Study for Treatment of Partial Seizures in Children | Phase3 | Partial Seizures | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00195780 | A Study for the Treatment of Mania Associated With Bipolar I Disorder in Childr… | Phase3 | Bipolar I Disorder | Completed | 2005-02-01 | — | ClinicalTrials.gov |
| NCT00424762 | Effect of Rosiglitazone Versus Placebo on Cardiovascular Performance and Myocar… | Phase4 | Diabetes Mellitus, Type 2 | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01749449 | Increased Dietary Protein and Meal Frequency Reduces Total and Abdominal Body F… | Na | Obesity | Completed | 2005-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00100685 | Study of M200 (Volociximab) in Patients With Metastatic Renal Cell Carcinoma (R… | Phase2 | Renal Cell Carcinoma | Terminated | 2005-01-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00234910 | Efficacy of Simplified Two Drug Kaletra Regimen vs. Kaletra Triple Drug Standar… | Phase3 | HIV Infection | Completed | 2005-01-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00569816 | Continuous Versus Repetitive Sevoflurane Administration for Preconditioning | Phase4 | Myocardial Injury | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00114933 | "OK 2004 Study" (Only Kaletra 2004 Study): Study to Evaluate Suspending Nucleos… | Phase4 | HIV Infection | Completed | 2005-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT01325922 | 50/50% Tilt and Tuned Defibrillation Waveform | Na | DFT Testing | Completed | 2005-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00237887 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-12-01 | — | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00286195 | Frontier Registry II Bifurcation Stent System Registry | Phase4 | Coronary Artery Disease | Withdrawn | 2004-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00686751 | Immune Effects of Vitamin D in Hemodialysis Patients | Phase2 | End Stage Renal Disease | Completed | 2004-12-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00187213 | B-Left HF: Biventricular Versus Left Univentricular Pacing With Implantable Car… | Na | Heart Failure | Completed | 2004-12-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00222352 | Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Test… | — | Angina, Unstable | Completed | 2004-12-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00747565 | Safety and Effectiveness of a Multifocal Intraocular Lens (IOL) | Na | Cataract | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00194025 | Valproate in Late Life Schizophrenia | Phase4 | Schizophrenia | Completed | 2004-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00225082 | SNAP: Switching Nucleoside Analogues Protocol - Lipoatrophy and Mitochondrial F… | — | HIV Infection | Completed | 2004-11-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00211822 | Functional Magnetic Resonance Imaging (fMRI) Studies in Pathological Gambling (… | — | Pathological Gambling | Terminated | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase3 | Fibroid Uterus | Completed | 2004-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00206843 | Rapid Emergency Department Heart Failure Outpatient Trial (REDHOT II) | Na | Heart Failure | Completed | 2004-11-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00093301 | Levosimendan Versus Dobutamine in Shock Patients | Phase2 | Cardiogenic Shock | Unknown | 2004-10-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00105300 | Study of the Human Anti-TNF Monoclonal Antibody Adalimumab for the Induction of… | Phase3 | Crohn's Disease | Completed | 2004-10-01 | — | ClinicalTrials.gov |
| NCT00180466 | PROSPECT: An Imaging Study in Patients With Unstable Atherosclerotic Lesions | — | Coronary Disease | Completed | 2004-10-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00256152 | Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients an… | Phase4 | Hypertension | Completed | 2004-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00148356 | Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteri… | Phase2 | Coronary Disease | Completed | 2004-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00735878 | Pharmacokinetic & Pharmacodynamic Study of ABT-751 With Carboplatin in Patients… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2004-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00202514 | Placebo Controlled Trial of Depakote ER in Alcohol Dependent Patients With Mood… | Phase2 | Alcoholism | Completed | 2004-09-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00195715 | Long-term Safety and Tolerability Study of Adalimumab in Subjects With Crohn's … | Phase3 | Crohn's Disease | Completed | 2004-09-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00073710 | Study to Evaluate the Effects of Zemplar Injection and Calcijex on Intestinal A… | Phase4 | Secondary Hyperparathyroidism | Completed | 2004-09-01 | — | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00194116 | Double-blind, Placebo-Controlled Divalproex Sodium ER in Bipolar I or Bipolar I… | Phase3 | Bipolar Disorder | Completed | 2004-09-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00235872 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00091975 | Zemplar® Capsule in Reducing Serum Intact Parathyroid Hormone Levels in Chronic… | Phase3 | Kidney Disease | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00404183 | A Study Comparing the Analgesic Efficacy and Safety of Extended Release Hydroco… | Phase2 | Pain | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00217477 | Paricalcitol and Gemcitabine in Treating Patients With Advanced Cancer | Phase1 | Unspecified Adult Solid Tumor, Protocol Specific | Completed | 2004-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00419055 | Outpatient Percutaneous Coronary Intervention | — | Coronary Artery Disease | Terminated | 2004-08-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00696059 | Humira in Rheumatoid Arthritis - Do Bone Erosions Heal? | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00195793 | A 16 Week Comparative Study of Fenofibrate Versus Ezetimibe as Add-on Therapy t… | Phase3 | Hyperlipidemia | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00234897 | Efficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2004-08-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195767 | Evaluate the Safety of Depakote Extended Release Tablets in the Treatment of Ma… | Phase3 | Bipolar I Disorder, Manic or Mixed | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT00195754 | A Phase III Open-Label, Multi-Center, Long-Term Extension Study of Depakote ER … | Phase3 | Migraines | Completed | 2004-07-01 | — | ClinicalTrials.gov |
| NCT01087710 | Effect of Medical Food on Reducing Asthma Symptoms in Asthmatic Children | Phase2 | Asthma | Completed | 2004-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00235001 | Russian Study of the Efficacy and Safety of Tarka in Patients With Hypertension | Phase4 | Hypertension | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT00234988 | A Phase IV, Multi-Center, Open-Label Trial of Sibutramine in Combination With a… | Phase4 | Obesity | Completed | 2004-06-01 | — | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01081873 | Study to Document Treatment Patterns and to Evaluate Leuprolide and Alternative… | — | Prostatic Neoplasm | Completed | 2004-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00200369 | Characterization of the Adherence Threshold for HIV Suppression of a Kaletra-ba… | — | HIV Infection | Completed | 2004-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00925197 | Patient International Normalised Ratio (INR) Self-Testing Program | Phase3 | Mechanical Aortic and/or Mitral Valve Replacement Operation | Completed | 2004-05-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00596661 | The TRIMAXX Coronary Stent Trial | Phase1 | Coronary Artery Disease | Completed | 2004-05-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00195676 | Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Chronic P… | Phase3 | Psoriasis | Completed | 2004-05-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00184951 | Pharmacokinetic Study of Rosuvastatin and Lopinavir/Ritonavir in HIV Patients | Phase2 | HIV Infections | Completed | 2004-04-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | Phase3 | Fibroid Uterus | Completed | 2004-04-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00145795 | A Research Study to See if a Change in Therapy for HIV Infection Can Improve th… | Phase4 | HIV Infections | Completed | 2004-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00208195 | Depakote ER Therapy for Mania Comorbid With Substance Abuse | Phase4 | Bipolar Disorder | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00234858 | Tarka vs. Hyzaar in Patients With Metabolic Syndrome (STAR) | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00197834 | Study of Depakote for Behavioral and Psychological Symptoms in Dementia | Phase1 | Dementia | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00233532 | Canadian Study of Trandolapril on Blood Pressure in Hypertensive Patients (TRAI… | Phase4 | Hypertension | Completed | 2004-03-01 | — | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01379703 | Multicountry, Multicenter Post-Marketing Observational Study of Clinical, Biolo… | — | HIV-1 Patients | Completed | 2004-02-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00563641 | Very Early Surfactant and NCPAP for Premature Infants With RDS | Phase3 | Respiratory Distress Syndrome | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00234871 | Tarka® vs. Lotrel® in Hypertensive, Diabetic Subjects With Renal Disease (TANDE… | Phase4 | Hypertension | Completed | 2004-01-01 | — | ClinicalTrials.gov |
| NCT00203528 | Divalproex ER vs. Risperidone for Bipolar Disorder With Comorbid Substance Use … | Phase4 | Substance Abuse | Completed | 2004-01-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00186186 | Depakote ER in Bipolar Depression | Phase4 | Depression, Bipolar | Completed | 2004-01-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00181727 | Study of Depakote ER for the Treatment of Mania in Children Ages 6-12 With Bipo… | Phase4 | Bipolar Disorder | Completed | 2004-01-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00085644 | Human Anti-tumor Necrosis Factor (TNF) Monoclonal Antibody Adalimumab in Subjec… | Phase3 | Ankylosing Spondylitis | Completed | 2004-01-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00180453 | SPIRIT FIRST Clinical Trial of the Abbott Vascular XIENCE V® Everolimus Eluting… | Phase3 | Coronary Artery Disease | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00075231 | A Simplified Kaletra® (Lopinavir/Ritonavir)-Based Therapy Versus a Sustiva® (Ef… | Phase2 | HIV Infections | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00234936 | Quality of Life Study With Adalimumab in Rheumatoid Arthritis | Phase3 | Rheumatoid Arthritis | Completed | 2003-12-01 | — | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00195819 | Safety and Efficacy of Adalimumab in Patients With Active Ankylosing Spondylitis | Phase3 | Ankylosing Spondylitis | Completed | 2003-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01086059 | OTIS Humira Pregnancy Registry | — | Crohn's Disease | Completed | 2003-11-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00645112 | A Comparison of Safety and Efficacy of Cefdinir Oral Suspension Versus Azithrom… | Phase4 | Acute Otitis Media | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645073 | Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment… | Phase4 | Acute Bacterial Sinusitis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00645892 | Extension Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate… | Phase2 | Psoriasis | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00211263 | Bipolar Disorder Research Study for Ages 12 and Older | Na | Bipolar Disorder | Completed | 2003-11-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00404391 | A Study Comparing the Analgesic Activity of Extended Release Hydrocodone/Acetam… | Phase2 | Pain | Completed | 2003-10-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00900549 | Evaluation of Resynchronization Therapy for Heart Failure | Phase4 | Heart Failure | Terminated | 2003-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00649922 | Assessment of the Effect of Adalimumab on Response to Influenza Virus and Pneum… | Phase4 | Rheumatoid Arthritis | Completed | 2003-10-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00193856 | RADAR Trial - Randomised Androgen Deprivation and Radiotherapy | Phase3 | Prostate Cancer | Completed | 2003-10-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00206817 | Rapid Assessment of Cardiac Markers for the Evaluation of Acute Coronary Syndro… | Phase4 | Acute Coronary Syndrome | Withdrawn | 2003-10-01 | — | ClinicalTrials.gov |
| NCT00476359 | A PK and Salvage Study for Children With HIV-infection | Phase4 | HIV Infections | Completed | 2003-10-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00186537 | Comparing Tricor, Avandia, or Weight Loss to Lower Cardiovascular Risk Factors … | Na | Insulin Resistance | Completed | 2003-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00073151 | A Study of ABT-751 in Patients With Non-Small Cell Lung Cancer | Phase2 | Non-Small Cell Lung Cancer | Completed | 2003-09-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating W… | Phase3 | Fibroid Uterus | Completed | 2003-09-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | Phase3 | Leiomyoma | Completed | 2003-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00578708 | Closure of Perimembranous Ventricular Septal Defects With The AMPLATZER® Membra… | Phase1 | Membranous Ventricular Septal Defects | Completed | 2003-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00234884 | Post-marketing Observational Study in Subjects With Rheumatoid Arthritis | — | Rheumatoid Arthritis | Completed | 2003-09-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00193674 | Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Wome… | Phase3 | Recurrent Miscarriage | Completed | 2003-09-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00208819 | A Comparison of Two Standard Therapies in the Management of Dementia With Agita… | Phase4 | Senile Dementia, Alzheimer Type | Completed | 2003-09-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00374075 | Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patie… | Phase1 | Spinal Muscular Atrophy | Completed | 2003-09-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00195689 | Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active … | Phase3 | Psoriatic Arthritis | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00278772 | Study of Divalproex Extended Release Monotherapy in Ambulatory Bipolar Spectrum… | Phase3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | Completed | 2003-08-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073112 | A Study of ABT-751 in Patients With Renal Cell Cancer | Phase2 | Renal Cell Cancer | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234923 | Efficacy and Safety of Kaletra Monotheraphy Compared to Kaletra Based Triple Th… | Phase3 | HIV Infection | Completed | 2003-08-01 | — | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00179335 | Comparative Pharmacokinetics (PK) Study of Efavirenz or Lopinavir/Ritonavir Bet… | — | HIV Infections | Completed | 2003-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00073138 | A Study of ABT-751 in Patients With Colorectal Cancer | Phase2 | Colorectal Cancer | Completed | 2003-08-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00073164 | Depakote ER Plus an Atypical Antipsychotic Vs. an Atypical Antipsychotic Alone … | Phase2 | Schizophrenia | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00206856 | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) | Phase4 | Heart Failure | Terminated | 2003-07-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00243438 | DaVinci Registry(Distinctly Assess Vision in Coronary Intervention) | — | Coronary Disease | Completed | 2003-07-01 | 2005-03-01 | ClinicalTrials.gov |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibro… | Phase2 | Uterine Fibroids | Completed | 2003-07-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00077779 | Adalimumab for the Induction and Maintenance of Clinical Remission in Subjects … | Phase3 | Crohn's Disease | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00067431 | A Study of the Safety and Efficacy of Depakote Sprinkle Capsules in the Treatme… | Phase3 | Partial Seizure Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00235859 | Adalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With Me… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00203242 | An Open Label Study Using Consecutive Intravenous Depacon With Oral Depakote ER… | Na | Cluster Headache | Completed | 2003-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00069849 | A Study of the Safety and Efficacy of Multiple Doses of ABT-089 in Subjects Wit… | Phase2 | Alzheimer's Disease | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00647920 | Study of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rh… | Phase3 | Rheumatoid Arthritis | Completed | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00071253 | Depakote Monotherapy, Olanzapine Monotherapy, and Combination Therapy of Depako… | Phase4 | Bipolar Disorder | Terminated | 2003-07-01 | — | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00646178 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase3 | Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00187187 | DAVID II (Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial II) | Na | Ventricular Tachycardia | Completed | 2003-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00091481 | Study to Compare Initial Dosing Parameters of Zemplar in Stage V Chronic Kidney… | Phase4 | Kidney Failure, Chronic | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00645905 | Study of Two Dosing Schedules of Adalimumab in Subjects With Moderate to Severe… | Phase2 | Psoriasis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00135460 | Comparing a Nucleoside-Analogue-Sparing Regimen and a Protease-Inhibitor-Sparin… | Phase4 | HIV-Associated Lipodystrophy Syndrome | Unknown | 2003-06-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00235833 | Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis | Phase2 | Rheumatoid Arthritis | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00187278 | Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardi… | Na | Atrioventricular Block | Completed | 2003-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00061659 | Study Evaluating the Safety and Efficacy of ABT-510 in Subjects With Locally Ad… | Phase2 | Sarcoma, Soft Tissue | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00073125 | Safety and Efficacy of ABT-510 in Subjects With Advanced Renal Cell Carcinoma | Phase2 | Carcinoma, Renal Cell | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00195741 | The Safety and Efficacy of Divalproex Sodium Extended-Release Tablets in Migrai… | Phase3 | Migraine | Completed | 2003-05-01 | — | ClinicalTrials.gov |
| NCT00064376 | Paricalcitol in Treating Patients With Myelodysplastic Syndrome | Phase2 | Leukemia | Completed | 2003-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00187265 | Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients | Na | Heart Failure | Completed | 2003-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00061672 | Study Evaluating the Safety and Effectiveness of ABT-510 in Subjects With Refra… | Phase2 | Lymphoma, Non-Hodgkin | Completed | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00062699 | Evaluate the Survival Benefits of Zemplar Versus Calcijex in Subjects w/ Stage … | Phase4 | End-Stage Kidney Disease | Terminated | 2003-04-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00061646 | Safety and Effectiveness of ABT-510 Plus Combination Chemotherapy in Subjects W… | Phase2 | Carcinoma, Non-Small-Cell Lung | Terminated | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00056654 | Study of a 6-Month Sustained-Release Formulation of Leuprolide Acetate in Prost… | Na | Prostatic Neoplasms | Completed | 2003-03-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00645814 | Multicenter Study of the Safety and Efficacy of Adalimumab in Subjects With Mod… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00234845 | Adalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheu… | Phase3 | Rheumatoid Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00348504 | Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic … | Phase3 | Acute Heart Failure | Completed | 2003-03-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00067262 | An Outpatient Study of the Effectiveness and Safety of Depakote ER in the Treat… | Phase3 | Bipolar Disorder | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646191 | Study of the Safety and Efficacy of Adalimumab in Subjects With Moderate to Sev… | Phase2 | Psoriasis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00222482 | Depakote ER in Borderline Personality Disorder | Na | Borderline Personality Disorder | Completed | 2003-03-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00646386 | Study of the Safety and Efficacy of the Human Anti-TNF Monoclonal Antibody Adal… | Phase2 | Arthritis | Completed | 2003-03-01 | — | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00646711 | Pediatric Switch Study for Children and Adolescent Patients With Epilepsy | Phase2 | Pediatric Epilepsy | Completed | 2003-02-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00644943 | A Comparison of the Safety and Efficacy of Cefdinir Oral Suspension Versus Amox… | Phase4 | Acute Otitis Media | Completed | 2003-02-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00645125 | A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amox… | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00122226 | MEDICLAS Study (Metabolic Effects of Different Classes of AntiretroviralS) | Phase4 | HIV Infections | Unknown | 2003-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00644891 | Pediatric Taste Test Study of Cefdinir (Omnicef) Versus Amoxicillin Antibiotic … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00060905 | An Inpatient Study of the Effectiveness and Safety of Depakote ER in the Treatm… | Phase3 | Bipolar Disorder | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00234832 | A Long Term Study of Sibutramine and the Role of Obesity Management in Relation… | Phase3 | Obesity | Completed | 2003-01-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00644774 | A Pediatric Taste Test Study of Omnicef Versus Zithromax Antibiotic Suspension … | Phase4 | Healthy | Completed | 2003-01-01 | — | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00160420 | A Long-Term Study to Evaluate the Safety of Asoprisnil in the Treatment of Wome… | Phase2 | Endometriosis | Completed | 2002-12-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00645086 | Comparative Study of 5 Days of M02-472 Clarithromycin Extended-Release Tablets … | Phase3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00677391 | Efficacy and Safety Study of Sibutramine in Overweight Non-Diabetic Malaysian P… | Phase3 | Obesity | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00063102 | A Study of ABT-751 in Patients With Recurrent Breast Cancer After Taxane (Taxol… | Phase2 | Breast Cancer | Completed | 2002-11-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00046943 | Atrasentan in Treating Patients With Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00448383 | A Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequat… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase3 | Leiomyoma | Completed | 2002-09-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00049751 | Study of Human Anti-TNF Monoclonal Antibody D2E7 in Subjects With Active Rheuma… | Phase3 | Rheumatoid Arthritis | Completed | 2002-09-01 | — | ClinicalTrials.gov |
| NCT00048542 | Study of Human Anti-TNF Monoclonal Antibody Adalimumab in Children With Polyart… | Phase3 | Arthritis, Juvenile Idiopathic | Completed | 2002-09-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00048425 | Evaluation of Intravenous Levosimendan Efficacy in the Short Term Treatment of … | Phase3 | Heart Failure, Congestive | Completed | 2002-09-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00234962 | Study of Adherence Effects and Clinical Outcomes of Kaletra Based HIV Antiviral… | Phase4 | HIV Infection | Terminated | 2002-08-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00160433 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Endometriosis | Completed | 2002-08-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00540488 | Glucose/Insulin Responses:Subjects With Type 2 Diabetes Consuming Diabetes-Spec… | Phase3 | Diabetes Mellitus Type 2 | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00055497 | Remission in Subjects With Crohn's Disease, 1 Year Phase | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01070303 | Remission in Subjects With Crohn's Disease, Open Label Extension | Phase3 | Crohn's Disease | Completed | 2002-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00309712 | Diabetes and Combined Lipid Therapy Regimen (DIACOR) Study | Na | Type II Diabetes Mellitus | Completed | 2002-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00043953 | Lopinavir/Ritonavir in Combination With Saquinavir Mesylate or Lamivudine/Zidov… | Phase2 | HIV Infections | Completed | 2002-08-01 | — | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00645203 | Safety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to… | Phase2 | Acute Otitis Media | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00043966 | Study of Lopinavir, Ritonavir, Tenofovir and Emtricitabine in HIV-Infected Anti… | Phase3 | HIV Infections | Completed | 2002-07-01 | — | ClinicalTrials.gov |
| NCT00919373 | Substrate Modification in Stable Ventricular Tachycardia in Addition to Implant… | Na | Ventricular Tachycardia | Completed | 2002-07-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | Phase3 | Leiomyoma | Completed | 2002-07-01 | 2005-01-01 | ClinicalTrials.gov |
| NCT01912326 | Prevention of Atrial Fibrillation by Optimized Overdrive Stimulation | Na | Bradycardia | Completed | 2002-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00354952 | Selection of Antibiotic Resistance by Azithromycin and Clarithromycin in the Or… | Na | Healthy Volunteers | Completed | 2002-07-01 | 2003-10-01 | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00122018 | An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents … | Phase2 | Kidney Failure, Acute | Completed | 2002-05-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00038662 | Safety and Efficacy of Atrasentan in Men With Hormone Naive Prostate Cancer Exh… | Phase2 | Prostatic Neoplasms | Completed | 2002-05-01 | — | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00143689 | NRTI-Sparing Pilot Study | Phase4 | HIV | Completed | 2002-04-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00417664 | Is Dexmedetomidine Associated With a Lower Incidence of Postoperative Delirium … | — | Delirium | Completed | 2002-04-01 | 2004-04-01 | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00055523 | A Study of the Human Anti-TNF Antibody Adalimumab for the Induction of Clinical… | Phase2 | Crohn's Disease | Completed | 2002-04-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048451 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00679653 | Blood Pressure and Weight Trajectory on a Dual Antihypertensive Combination Plu… | Phase3 | Obesity | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048516 | Safety and Efficacy of Zemplar Capsule in Reducing Serum iPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00180583 | Vision II: Evaluation of GALILEO Intravascular Radiotherapy System | Phase4 | Coronary Artery Disease | Completed | 2002-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00048438 | Safety and Efficacy of Zemplar Capsule in Reducing Serum IPTH Levels in Chronic… | Phase3 | Renal Insufficiency, Chronic | Completed | 2002-02-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053378 | A Study to Examine the Use of Zemplar to Increase Serum Calcium Levels in ICU S… | Phase2 | Hypocalcemia | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00053547 | Safety and Effectiveness of Zemplar Injection in Decreasing iPTH Levels in Pedi… | Phase4 | Secondary Hyperparathyroidism | Completed | 2002-01-01 | — | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00181558 | Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone | Phase2 | Prostate Cancer | Completed | 2001-12-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00202319 | Effectiveness of Sedation Management in an Australian Intensive Care Unit | Na | Respiration Disorders | Completed | 2001-11-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00127478 | A Long Term Safety Study With Atrasentan | Phase2 | Prostate Cancer | Completed | 2001-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00036556 | Study of Atrasentan in Men With Non-Metastatic, Hormone-Refractory Prostate Can… | Phase3 | Prostatic Neoplasms | Completed | 2001-06-01 | — | ClinicalTrials.gov |
| NCT01083810 | Evaluation of Kaletra Therapy Over the Long-term | — | Human Immunodeficiency Virus | Completed | 2001-06-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00715273 | Evaluate Carotid Artery Plaque Composition by Magnetic Resonance Imaging in Peo… | Phase4 | Coronary Artery Disease | Completed | 2001-05-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00036543 | A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer | Phase3 | Prostate Cancer | Completed | 2001-05-01 | — | ClinicalTrials.gov |
| NCT00032435 | Homocysteine Study (HOST) | Phase3 | End Stage Renal Disease | Completed | 2001-05-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01153269 | Long-term Effectiveness and Safety in Hepatitis-co-infected Patients | — | Human Immunodeficiency Virus-Infection | Completed | 2001-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038519 | Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00038532 | Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Subject… | Phase2 | HIV Infections | Completed | 2001-04-01 | — | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | Phase2 | Leiomyoma | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00152295 | A Long-Term Study to Evaluate the Safety of Asoprisnil and Estrogen Administrat… | Phase2 | Postmenopause | Completed | 2001-04-01 | 2001-12-01 | ClinicalTrials.gov |
| NCT00187291 | Study to Compare TWA Test and EPS Test for Predicting Patients at Risk for Life… | Phase3 | Ischemic Cardiomyopathy | Completed | 2001-04-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00262717 | Can Resistance Enhance Selection of Treatment? (CREST) | Na | HIV Infection | Completed | 2001-03-01 | 2006-07-31 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00422396 | Effects of Micronized Fenofibrate on Fasting and Postprandial Lipoproteins, Inf… | Na | Hypertriglyceridemia With the Metabolic Syndrome | Completed | 2001-01-01 | 2002-04-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00257959 | Optimal Pharmacological Therapy In Implantable Defibrillator Patients (OPTIC) | Phase4 | Ventricular Tachycardia | Completed | 2001-01-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00304993 | Study of Niacin and Rosiglitazone in Dysmetabolic Dyslipidemia | Phase4 | Metabolic Syndrome X | Completed | 2001-01-01 | 2005-02-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076985 | Special Investigation of Kaletra in Pregnant Women | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT01076972 | Drug Use Investigation of Kaletra | — | Human Immunodeficiency Virus | Completed | 2000-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT00205634 | Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis | Phase2 | Cystic Fibrosis | Completed | 2000-12-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00272103 | Itopride in Functional Dyspepsia:a Dose Finding Study | Phase2 | Functional Dyspepsia | Completed | 2000-12-01 | 2002-01-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT01820494 | Nutritional Management of Infants With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 2000-10-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00152282 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil and Estrogen Adm… | Phase2 | Amenorrhea | Completed | 2000-09-01 | 2001-08-01 | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00038636 | A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Wh… | Phase3 | HIV Infections | Completed | 2000-09-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00402584 | A Study to Examine the Efficacy and Safety of Meridia® (Sibutramine Hydrochlori… | Phase3 | Binge Eating Disorder | Completed | 2000-08-01 | — | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00583791 | Closure of Muscular Ventricular Septal Defects With The AMPLATZER™ Muscular VSD… | Na | Heart Septal Defects, Ventricular | Completed | 2000-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00038220 | Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovi… | Phase2 | HIV Infections | Completed | 2000-07-01 | — | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195650 | Long Term Open Label Continuation Study | Phase3 | Rheumatoid Arthritis | Completed | 2000-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00180544 | Safety and Effectiveness Study of the HERCULINK 14 Stent to Treat Renal Artery … | Phase3 | Renal Artery Obstruction | Terminated | 2000-07-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00261911 | A Study of Sibutramine in Overweight Adolescents to Assess Weight Loss and Safe… | Phase3 | Obesity | Completed | 2000-07-01 | 2002-02-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00233571 | A Long Term Roll-over Study to Investigate the Efficacy and Safety of Adalimuma… | Phase3 | Rheumatoid Arthritis | Completed | 2000-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment… | Phase2 | Leiomyoma | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00180518 | ACCULINK for Revascularization of Carotids in High Risk Patients "The ARCHeR Tr… | Phase2 | Carotid Atherosclerosis | Completed | 2000-05-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00160446 | A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in t… | Phase2 | Endometriosis | Completed | 2000-05-01 | 2001-07-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00269386 | Clarithromycin in Active Crohn's Disease | Phase3 | Crohn's Disease | Completed | 2000-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00195702 | Efficacy and Safety of Adalimumab in Patients With Active Rheumatoid Arthritis … | Phase3 | Rheumatoid Arthritis | Completed | 2000-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00166257 | PC-Trial: Patent Foramen Ovale and Cryptogenic Embolism | Phase4 | Embolism, Paradoxical | Unknown | 2000-02-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT01813526 | Infants With Protein Sensitive Colitis | Na | Protein Sensitive Colitis | Completed | 1999-11-01 | 2001-02-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00306852 | Tube Versus Trabeculectomy (TVT) Study | Na | Glaucoma | Completed | 1999-10-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT00121550 | The CLARICOR Trial: Effect of Clarithromycin on Mortality and Morbidity in Pati… | Phase3 | Heart Disease | Completed | 1999-10-01 | 2002-09-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT01699386 | Growth of Infants Fed an Elemental Medical Food | Phase3 | Healthy Infants | Completed | 1999-04-01 | 2000-12-01 | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00004583 | A Phase III Study Comparing Two Different Anti-HIV Drug Combinations in HIV-Pos… | Phase3 | HIV Infections | Completed | 1999-03-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00645255 | Study to Examine the Longer-Term Efficacy and Safety of Sibutramine Hydrochlori… | Phase3 | Obesity | Terminated | 1998-09-01 | — | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00590889 | Artificial Valve Endocarditis Reduction Trial | Na | Aortic Valve Disease | Terminated | 1998-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00194129 | Lithium and Divalproex for the Treatment of Comorbid Rapid Cycling Bipolar Diso… | Phase3 | Bipolar Disorder | Completed | 1997-11-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00004578 | ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antir… | Phase1 | HIV Infections | Completed | 1997-11-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00133692 | INVEST: INternational VErapamil SR Trandolapril STudy | Phase4 | Hypertension | Completed | 1997-09-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT01812629 | Nutritional Management of Children With Chronic Diarrhea | Na | Growth and Tolerance Infant Study | Completed | 1997-07-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00235014 | A Study for Prevention of Kidney Disease in Diabetic Patients (BENEDICT) | Phase4 | Hypertension | Completed | 1997-03-01 | — | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00598897 | Use of Clarithromycin and Rifabutin for the Treatment of M. Avium Complex (MAC)… | Phase4 | Mycobacterium Avium Complex Lung Disease | Completed | 1995-08-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT00002331 | The Safety and Effectiveness of Clarithromycin Plus Ethambutol Used With or Wit… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1994-01-01 | 1995-03-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT02456831 | Soy Formula Feedings in Healthy, Term Infants | Na | Gastrointestinal Tolerance | Completed | 1992-12-01 | 1994-06-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT00002336 | The Safety and Effectiveness of Clarithromycin in the Prevention of Mycobacteri… | Na | Mycobacterium Avium-intracellular Infection | Completed | 1992-11-01 | 1994-11-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT02066610 | Effect of Selenium Supplementation on Trace Mineral Antioxidant Enzyme and Amin… | Na | Preterm Infants | Completed | 1991-03-01 | 1993-06-01 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00600769 | Clarithromycin for the Treatment of Infections Caused by Nontuberculous Mycobac… | Phase4 | Nontuberculous Mycobacteria | Completed | 1991-01-01 | 2017-05-18 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00660010 | Study of Lupron Depot In The Treatment of Central Precocious Puberty | Phase3 | Puberty, Precocious | Completed | 1991-01-01 | 2009-04-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Navitor Titan Valve (35mm) Valve and Large FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Portico™ NG (Navitor) Valve and FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| FFR>0.80+ OCT with findings indicative of vulnerable plaque | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05599061 |
| AVEIR CSP Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker | RECRUITING | NCT07287423 |
| Navitor Transcatheter Aortic Valve, FlexNav Delivery System, Navitor Loading System | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06008080 |
| Prospective, single-arm, multi-center study. | Other | Approved | Severe Native Calcific Aortic Stenosis | NOT_YET_RECRUITING | NCT07696182 |
| LBBAP with SyncAV | Other | Preclinical | Heart Failure | RECRUITING | NCT06436053 |
| CardioMEMS HF System | Other | Preclinical | Heart Failure NYHA Class II | ENROLLING_BY_INVITATION | NCT06306573 |
| Epic™ Surgical Tissue Heart Valve devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Amplatzer™ Occlusion Devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Cephea Mitral Valve System | Other | Approved | Mitral Regurgitation | RECRUITING | NCT05061004 |
| Esprit BTK™ Everolimus Eluting Resorbable Scaffold from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270575 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | RECRUITING | NCT07586995 |
| Left Atrial Appendage (LAA) closure procedure with Amplatzer Amulet LAA occluder | Procedure | Preclinical | Non-Valvular Atrial Fibrillation | TERMINATED | NCT06189365 |
| Esprit BTK™ Everolimus Eluting Resorbable Scaffold from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270575 |
| Stealth 360™ Peripheral Orbital Atherectomy System from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270562 |
| Grid X and EnSite X v3.1.1 Software | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | RECRUITING | NCT07421076 |
| Experimental Nutrition Product | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT07426406 |
| CardioMEMS | Other | Approved | Heart Failure With Reduced Ejection Fraction | RECRUITING | NCT06241430 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Open loop | Other | Approved | Type 2 Diabetes | RECRUITING | NCT06959797 |
| Closed loop | Other | Approved | Type 2 Diabetes | RECRUITING | NCT06959797 |
| antegrade and retrograde approach | Other | Preclinical | Chronic Total Occlusion of Coronary Artery | RECRUITING | NCT03667196 |
| Caloric restriction | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07666581 |
| Glucerna | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07666581 |
| Anatomical midline lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| Paresthesia mapping lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| DBS of the NAc | Other | Approved | Opioid-use Disorder | RECRUITING | NCT04354077 |
| MitraClip System | Other | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03433274 |
| Tendyne Mitral Valve System | Other | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03433274 |
| Veliparib | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Pharmacological Study | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Paclitaxel | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Carboplatin | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Experimental | Other | Approved | Coronary Artery Calcification | ACTIVE_NOT_RECRUITING | NCT06885177 |
| EverFlex™ Self-Expanding Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT03941314 |
| Supera® Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT03941314 |
| Guideline Medical Directed Therapy | Drug | Approved | Heart Failure | RECRUITING | NCT06526195 |
| HeartMate 3 Left Ventricular Assist System | Other | Approved | Heart Failure | RECRUITING | NCT06526195 |
| CardioMEMS HF System | Other | Approved | Heart Failure | RECRUITING | NCT06526195 |
| Implantable Loop Recorder | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT07638995 |
| Navitor Titan Valve (35mm) Valve and Large FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Portico™ NG (Navitor) Valve and FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Atrial Fibrillation Radiofrequency Ablation Only | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07441382 |
| catheter ablation combined with LAAO (Left Atrial Appendage Occlusion) | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07441382 |
| ICM Implantation | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| Standard of Care | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| Continuous glucose monitoring using a wearable sensor (flash interstitial glucose monitor) | Other | Preclinical | Prediabetes (Insulin Resistance, Impaired Glucose Tolerance) | NOT_YET_RECRUITING | NCT07626658 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Directional Deep Brain Stimulation of STN | Other | Approved | Parkinson Disease | COMPLETED | NCT03548506 |
| Omnidirectional Deep Brain Stimulation of STN | Other | Approved | Parkinson Disease | COMPLETED | NCT03548506 |
| PCI revascularization strategy based FFR assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| PCI revascularization strategy based on combined FFR and OCT assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | RECRUITING | NCT07599982 |
| Routine Care | Other | Approved | PreDiabetes | COMPLETED | NCT05580978 |
| GEM | Other | Approved | PreDiabetes | COMPLETED | NCT05580978 |
| Amulet™ 2 Left Atrial Appendage (LAA) Occluder | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT06707688 |
| Transseptal procedure with Agilis RF TSP System. | Procedure | Approved | Cardiac Arrythmias | RECRUITING | NCT07361445 |
| ViewFlex X ICE System | Other | Preclinical | Cardiac Arrhythmias | RECRUITING | NCT06772493 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation | NOT_YET_RECRUITING | NCT07621003 |
| Amplatzer PFO Occluder | Other | Preclinical | PFO - Patent Foramen Ovale | COMPLETED | NCT04349995 |
| PFA Ablation catheter | Other | Approved | Atrial Fibrillation (AF) | COMPLETED | NCT06676072 |
| protein supplement | Other | Approved | Type 2 Diabetes | RECRUITING | NCT07271043 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | RECRUITING | NCT07599982 |
| Drug-eluting stent | Drug | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Angiography-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| OCT-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Tendyne™ Mitral Valve System | Other | Preclinical | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04818502 |
| Continuous glucose monitoring | Other | Approved | Type 2 Diabetes Mellitus (T2DM) | ACTIVE_NOT_RECRUITING | NCT06888687 |
| Dietetic support | Other | Approved | Type 2 Diabetes Mellitus (T2DM) | ACTIVE_NOT_RECRUITING | NCT06888687 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Left Atrial Appendage Occluder Implant | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| PVI Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07523620 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Aveir DR Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker, Artificial | COMPLETED | NCT05252702 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Intralesional Tranexamic Acid | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Mandelic Acid Peel | Other | Approved | Melasma | NOT_YET_RECRUITING | NCT07604844 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT05270499 |
| MODI Algorithm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07599982 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | COMPLETED | NCT04559945 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Self monitoring of blood glucose | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| FreeStyle Libre 3 Continuous Glucose Monitoring System. | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05944432 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Risperidone | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Olanzapine | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Divalproex Sodium Extended-Release Tablets | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Risperidone | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Olanzapine | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Divalproex Sodium Extended-Release Tablets | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT00073164 |
| Olanzapine | Other | Phase PHASE4 | Bipolar Disorder | TERMINATED | NCT00071253 |
| Divalproex Sodium (Extended-Release Tablets) | Other | Phase PHASE4 | Bipolar Disorder | TERMINATED | NCT00071253 |
| Divalproex Sodium (Delayed-Release Tablets) | Other | Phase PHASE4 | Bipolar Disorder | TERMINATED | NCT00071253 |
| Divalproex Sodium (Depakote® Sprinkle Capsules) | Other | Phase PHASE3 | Partial Seizure Disorder | TERMINATED | NCT00067431 |
| Divalproex Sodium (Depakote® Sprinkle Capsules) | Other | Phase PHASE3 | Partial Seizure Disorder | TERMINATED | NCT00067431 |
| Divalproex Sodium Extended-Release Tablets | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00067262 |
| Divalproex Sodium Extended-Release Tablets | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00067262 |
| Divalproex Sodium (Depakote ER) | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00060905 |
| Zemplar | Other | Phase PHASE4 | Kidney Failure, Chronic | COMPLETED | NCT00091481 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00077779 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00077779 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00338650 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00338650 |
| Atrasentan | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00127478 |
| Atrasentan | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00127478 |
| ABT-751 | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | COMPLETED | NCT00073151 |
| ABT-751 | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | COMPLETED | NCT00073151 |
| ABT-751 | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT00073138 |
| ABT-751 | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT00073138 |
| ABT-751 | Other | Phase PHASE2 | Renal Cell Cancer | COMPLETED | NCT00073112 |
| ABT-751 | Other | Phase PHASE2 | Breast Cancer | COMPLETED | NCT00063102 |
| ABT-751 | Other | Phase PHASE2 | Breast Cancer | COMPLETED | NCT00063102 |
| ABT-510 - Thrombospondin-1 mimetic | Other | Phase PHASE2 | Sarcoma, Soft Tissue | COMPLETED | NCT00061659 |
| ABT-510 - Thrombospondin-1 mimetic | Other | Phase PHASE2 | Sarcoma, Soft Tissue | COMPLETED | NCT00061659 |
| Depakote DR | Other | Phase PHASE4 | Mania | COMPLETED | NCT00334347 |
| Depakote ER | Other | Phase PHASE4 | Mania | COMPLETED | NCT00334347 |
| Depakote DR | Other | Phase PHASE4 | Mania | COMPLETED | NCT00334347 |
| Depakote ER | Other | Phase PHASE4 | Mania | COMPLETED | NCT00334347 |
| Sevoflurane | Other | Phase PHASE4 | Myocardial Injury | COMPLETED | NCT00569816 |
| Dobutamine | Other | Phase PHASE2 | Cardiogenic Shock | UNKNOWN | NCT00093301 |
| Levosimendan | Other | Phase PHASE2 | Cardiogenic Shock | UNKNOWN | NCT00093301 |
| Sedation management protocol | Other | Approved | Respiration Disorders | COMPLETED | NCT00202319 |
| Sedation management protocol | Other | Approved | Respiration Disorders | COMPLETED | NCT00202319 |
| Adalimumab 40 mg sc every other week | Other | Phase PHASE2 | Ankylosing Spondylitis | UNKNOWN | NCT00235105 |
| Adalimumab 40 mg sc every other week | Other | Phase PHASE2 | Ankylosing Spondylitis | UNKNOWN | NCT00235105 |
| Adalimumab 40 mg sc every other week | Other | Phase PHASE2 | Ankylosing Spondylitis | UNKNOWN | NCT00235105 |
| nucleoside analogue sparing HAART regimen | Other | Phase PHASE4 | HIV-Associated Lipodystrophy Syndrome | UNKNOWN | NCT00135460 |
| nucleoside analogue sparing HAART regimen | Other | Phase PHASE4 | HIV-Associated Lipodystrophy Syndrome | UNKNOWN | NCT00135460 |
| nucleoside analogue sparing HAART regimen | Other | Phase PHASE4 | HIV-Associated Lipodystrophy Syndrome | UNKNOWN | NCT00135460 |
| Rapid versus slow conversion | Other | Phase PHASE4 | Epilepsy | UNKNOWN | NCT00312676 |
| Rapid versus slow conversion | Other | Phase PHASE4 | Epilepsy | UNKNOWN | NCT00312676 |
| Lopinavir/ritonavir + nevirapine | Other | Phase PHASE4 | HIV Infections | UNKNOWN | NCT00122226 |
| Lopinavir/ritonavir + zidovudine + lamivudine | Other | Phase PHASE4 | HIV Infections | UNKNOWN | NCT00122226 |
| Lopinavir/ritonavir + nevirapine | Other | Phase PHASE4 | HIV Infections | UNKNOWN | NCT00122226 |
| Lopinavir/ritonavir + zidovudine + lamivudine | Other | Phase PHASE4 | HIV Infections | UNKNOWN | NCT00122226 |
| Itopride (drug) | Drug | Phase PHASE2 | Functional Dyspepsia | COMPLETED | NCT00272103 |
| Itopride (drug) | Drug | Phase PHASE2 | Functional Dyspepsia | COMPLETED | NCT00272103 |
| Macrolides (azithromycin or clarithromycin) | Other | Approved | Healthy Volunteers | COMPLETED | NCT00354952 |
| Macrolides (azithromycin or clarithromycin) | Other | Approved | Healthy Volunteers | COMPLETED | NCT00354952 |
| amiodarone beta blocker sotalol | Other | Phase PHASE4 | Ventricular Tachycardia | COMPLETED | NCT00257959 |
| Truvada (emtricitabine/tenofovir disoproxil fumarate) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Sustiva (efavirenz) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Kaletra (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Truvada (emtricitabine/tenofovir disoproxil fumarate) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Sustiva (efavirenz) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Kaletra (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Truvada (emtricitabine/tenofovir disoproxil fumarate) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Sustiva (efavirenz) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Kaletra (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infection | WITHDRAWN | NCT00121017 |
| Emtricitabine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00043966 |
| Tenofovir DF | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00043966 |
| Lopinavir/ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00043966 |
| Tenofovir DF | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Lamivudine | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Efavirenz | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Tenofovir DF | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Lamivudine | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Efavirenz | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038220 |
| Saquinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038519 |
| Amprenavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038519 |
| Saquinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038519 |
| Amprenavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038519 |
| Calcijex | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| 42 Ca carbonate absorption via single tracer method | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Zemplar | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Calcijex | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| 42 Ca carbonate absorption via single tracer method | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Zemplar | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Calcijex | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| 42 Ca carbonate absorption via single tracer method | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Zemplar | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00073710 |
| Calcijex | Other | Phase PHASE4 | End-Stage Kidney Disease | TERMINATED | NCT00062699 |
| Zemplar (paricalcitol injection) | Other | Phase PHASE4 | End-Stage Kidney Disease | TERMINATED | NCT00062699 |
| Calcijex | Other | Phase PHASE4 | End-Stage Kidney Disease | TERMINATED | NCT00062699 |
| Zemplar (paricalcitol injection) | Other | Phase PHASE4 | End-Stage Kidney Disease | TERMINATED | NCT00062699 |
| paricalcitol injection | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00053547 |
| paricalcitol injection | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00053547 |
| paricalcitol injection | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00053547 |
| Administration of elemental Ca during hypocalcemic ICU pts. | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| Effects on calcium regulation | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| paricalcitol injection (Zemplar) | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| Administration of elemental Ca during hypocalcemic ICU pts. | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| Effects on calcium regulation | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| paricalcitol injection (Zemplar) | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| Administration of elemental Ca during hypocalcemic ICU pts. | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| Effects on calcium regulation | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| paricalcitol injection (Zemplar) | Other | Phase PHASE2 | Hypocalcemia | COMPLETED | NCT00053378 |
| paricalcitol capsule | Other | Phase PHASE3 | Renal Insufficiency, Chronic | COMPLETED | NCT00048516 |
| paricalcitol capsule | Other | Phase PHASE3 | Renal Insufficiency, Chronic | COMPLETED | NCT00048516 |
| paricalcitol | Other | Phase PHASE3 | Renal Insufficiency, Chronic | COMPLETED | NCT00048451 |
| paricalcitol | Other | Phase PHASE3 | Renal Insufficiency, Chronic | COMPLETED | NCT00048451 |
| Depakote | Other | Phase PHASE1 | Dementia | UNKNOWN | NCT00197834 |
| Depakote | Other | Phase PHASE1 | Dementia | UNKNOWN | NCT00197834 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00105300 |
| Adalimumab (D2E7) | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT00055523 |
| Adalimumab (D2E7) | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT00055523 |
| Adalimumab (D2E7) | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT00055523 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00049751 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00049751 |
| paricalcitol | Other | Phase PHASE3 | Renal Insufficiency, Chronic | COMPLETED | NCT00048438 |
| Atrasentan | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00038662 |
| Atrasentan | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00038662 |
| Atrasentan | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00038662 |
| Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00038636 |
| Lopinavir/ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00038636 |
| Atrasentan | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00036543 |
| Atrasentan | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00036543 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00069849 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00069849 |
| Kaletra (drug) | Drug | Approved | HIV | UNKNOWN | NCT00247143 |
| Sustiva® (efavirenz) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Combivir® (lamivudine, zidovudine) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Kaletra® (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Sustiva® (efavirenz) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Combivir® (lamivudine, zidovudine) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Kaletra® (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Sustiva® (efavirenz) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Combivir® (lamivudine, zidovudine) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Kaletra® (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00075231 |
| Levosimendan | Other | Phase PHASE3 | Heart Failure, Congestive | COMPLETED | NCT00048425 |
| Levosimendan | Other | Phase PHASE3 | Heart Failure, Congestive | COMPLETED | NCT00048425 |
| Levosimendan | Other | Phase PHASE3 | Heart Failure, Congestive | COMPLETED | NCT00048425 |
| divalproex sodium | Other | Phase PHASE3 | Migraine | COMPLETED | NCT00195741 |
| divalproex sodium | Other | Phase PHASE3 | Migraine | COMPLETED | NCT00195741 |
| risperidone | Other | Phase PHASE4 | Substance Abuse | COMPLETED | NCT00203528 |
| divalproex sodium ER | Other | Phase PHASE4 | Substance Abuse | COMPLETED | NCT00203528 |
| risperidone | Other | Phase PHASE4 | Substance Abuse | COMPLETED | NCT00203528 |
| divalproex sodium ER | Other | Phase PHASE4 | Substance Abuse | COMPLETED | NCT00203528 |
| divalproex sodium | Other | Phase PHASE3 | Bipolar I Disorder, Manic or Mixed | COMPLETED | NCT00195767 |
| divalproex sodium | Other | Phase PHASE3 | Bipolar I Disorder, Manic or Mixed | COMPLETED | NCT00195767 |
| divalproex sodium | Other | Phase PHASE3 | Bipolar I Disorder, Manic or Mixed | COMPLETED | NCT00195767 |
| methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00233558 |
| adalimumab (up to 9 months exposure) | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00233558 |
| methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00233558 |
| adalimumab (up to 9 months exposure) | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00233558 |
| Divalproex Sodium (Depakote Sprinkle Capsules) | Other | Phase PHASE3 | Partial Seizures | COMPLETED | NCT00102713 |
| Divalproex Sodium (Depakote ER) | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT00195780 |
| Divalproex Sodium (Depakote ER) | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT00195780 |
| Divalproex Sodium (Depakote ER) | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT00195780 |
| divalproex sodium | Other | Phase PHASE3 | Migraines | COMPLETED | NCT00195754 |
| Depakote ER | Other | Approved | Borderline Personality Disorder | COMPLETED | NCT00222482 |
| Depakote ER | Other | Approved | Borderline Personality Disorder | COMPLETED | NCT00222482 |
| Depakote ER | Other | Approved | Borderline Personality Disorder | COMPLETED | NCT00222482 |
| Carboplatin/Taxol | Other | Phase PHASE2 | Carcinoma, Non-Small-Cell Lung | TERMINATED | NCT00061646 |
| ABT-510/Thrombospondin-1 mimetic | Other | Phase PHASE2 | Carcinoma, Non-Small-Cell Lung | TERMINATED | NCT00061646 |
| WaterWorks Douching Device | Device | Approved | Vaginal Odor | UNKNOWN | NCT00417365 |
| WaterWorks Douching Device | Device | Approved | Vaginal Odor | UNKNOWN | NCT00417365 |
| ABT-510/Thrombospondin-1 mimetic | Other | Phase PHASE2 | Carcinoma, Renal Cell | COMPLETED | NCT00073125 |
| ABT-510/Thrombospondin-1 mimetic | Other | Phase PHASE2 | Carcinoma, Renal Cell | COMPLETED | NCT00073125 |
| ABT-510/Thrombospondin-1 mimetic | Other | Phase PHASE2 | Carcinoma, Renal Cell | COMPLETED | NCT00073125 |
| ABT-510 - Thrombospondin-1 Mimetic | Other | Phase PHASE2 | Lymphoma, Non-Hodgkin | COMPLETED | NCT00061672 |
| ABT-510 - Thrombospondin-1 Mimetic | Other | Phase PHASE2 | Lymphoma, Non-Hodgkin | COMPLETED | NCT00061672 |
| Atrasentan | Other | Phase PHASE3 | Prostatic Neoplasms | COMPLETED | NCT00036556 |
| Atrasentan | Other | Phase PHASE3 | Prostatic Neoplasms | COMPLETED | NCT00036556 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00237887 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00237887 |
| adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00235885 |
| adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00235885 |
| methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00235859 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00235859 |
| methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00235859 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00235859 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00234897 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00234897 |
| methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234845 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234845 |
| Human anti-TNF monoclonal antibody/adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00195689 |
| Human anti-TNF monoclonal antibody/adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00195689 |
| sibutramine | Other | Phase PHASE3 | Binge Eating Disorder | COMPLETED | NCT00402584 |
| sibutramine | Other | Phase PHASE3 | Binge Eating Disorder | COMPLETED | NCT00402584 |
| sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00261911 |
| sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00261911 |
| divalproex sodium | Other | Phase PHASE3 | Migraine | COMPLETED | NCT00195806 |
| divalproex sodium | Other | Phase PHASE3 | Migraine | COMPLETED | NCT00195806 |
| Human anti-TNF monoclonal antibody adalimumab/ up to 24 weeks | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00338754 |
| Human anti-TNF monoclonal antibody adalimumab/ up to 24 weeks | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00338754 |
| Lamivudine/zidovudine | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Saquinavir mesylate | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Lamivudine/zidovudine | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Saquinavir mesylate | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Lamivudine/zidovudine | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Saquinavir mesylate | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00043953 |
| Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234936 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234936 |
| Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234936 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00234936 |
| atorvastatin | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00195793 |
| ezetimibe | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00195793 |
| fenofibrate | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00195793 |
| adalimumab (Humira) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00478660 |
| adalimumab (Humira) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00478660 |
| adalimumab (Humira) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00478660 |
| daily enteral nutritional product and/or behavioral changes | Other | Phase PHASE4 | Diabetes Mellitus, Type 2 | COMPLETED | NCT00543621 |
| Adult enteral formula | Other | Phase PHASE3 | Diabetes Mellitus Type 2 | COMPLETED | NCT00540488 |
| cephalexin | Other | Phase PHASE4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | COMPLETED | NCT00234949 |
| cefdinir | Other | Phase PHASE4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | COMPLETED | NCT00234949 |
| cephalexin | Other | Phase PHASE4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | COMPLETED | NCT00234949 |
| cefdinir | Other | Phase PHASE4 | Mild to Moderate Uncomplicated Skin and Skin Structure Infections | COMPLETED | NCT00234949 |
| Vicodin® CR (extended-release hydrocodone/acetaminophen) | Other | Phase PHASE1 | Drug Interactions | COMPLETED | NCT00429468 |
| Vicodin® CR (extended-release hydrocodone/acetaminophen) | Other | Phase PHASE1 | Drug Interactions | COMPLETED | NCT00429468 |
| Humira (adalimumab) | Other | Phase PHASE2 | Asthma | WITHDRAWN | NCT00512863 |
| Humira (adalimumab) | Other | Phase PHASE2 | Asthma | WITHDRAWN | NCT00512863 |
| dobutamine | Other | Phase PHASE3 | Acute Heart Failure | COMPLETED | NCT00348504 |
| levosimendan | Other | Phase PHASE3 | Acute Heart Failure | COMPLETED | NCT00348504 |
| dobutamine | Other | Phase PHASE3 | Acute Heart Failure | COMPLETED | NCT00348504 |
| levosimendan | Other | Phase PHASE3 | Acute Heart Failure | COMPLETED | NCT00348504 |
| bubble NCPAP | Other | Phase PHASE3 | Respiratory Distress Syndrome | COMPLETED | NCT00563641 |
| Very early surfactant and bubble NCPAP | Other | Phase PHASE3 | Respiratory Distress Syndrome | COMPLETED | NCT00563641 |
| bubble NCPAP | Other | Phase PHASE3 | Respiratory Distress Syndrome | COMPLETED | NCT00563641 |
| Very early surfactant and bubble NCPAP | Other | Phase PHASE3 | Respiratory Distress Syndrome | COMPLETED | NCT00563641 |
| Divalproex ER | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00208195 |
| Divalproex ER | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00208195 |
| suture mediated closure | Other | Preclinical | Cardiac Catheterization | UNKNOWN | NCT00838175 |
| Nevirapine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004580 |
| Lopinavir/Ritonavir | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004580 |
| Nevirapine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004580 |
| Lopinavir/Ritonavir | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004580 |
| Ritonavir | Other | Phase PHASE2 | Sarcoma, Kaposi | COMPLETED | NCT00002366 |
| Ritonavir | Other | Phase PHASE2 | Sarcoma, Kaposi | COMPLETED | NCT00002366 |
| placebo for adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645905 |
| adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645905 |
| placebo for adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645892 |
| adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645892 |
| adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645814 |
| placebo for adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645814 |
| Adalimumab (Humira) | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00696059 |
| Adalimumab (Humira) | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00696059 |
| Guidant GALILEO Intravascular Radiotherapy System | Drug | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00180583 |
| Guidant GALILEO Intravascular Radiotherapy System | Drug | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00180583 |
| RX ACCULINK(TM) Carotid Stent System and RX ACCUNET(TM) Embolic Protection System | Other | Approved | Atherosclerotic Disease, Carotid | COMPLETED | NCT00180492 |
| Stavudine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Lamivudine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Nelfinavir mesylate | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Lopinavir/Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Stavudine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Lamivudine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Nelfinavir mesylate | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Lopinavir/Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004583 |
| Nevirapine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Lopinavir/Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Nevirapine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Lopinavir/Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Nevirapine | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Lopinavir/Ritonavir | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00004581 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002275 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002275 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002275 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002275 |
| Ritonavir | Other | Approved | HIV Infections | COMPLETED | NCT00002223 |
| Indinavir sulfate | Other | Approved | HIV Infections | COMPLETED | NCT00002223 |
| Nelfinavir mesylate | Other | Approved | HIV Infections | COMPLETED | NCT00002201 |
| Ritonavir | Other | Approved | HIV Infections | COMPLETED | NCT00002201 |
| Aspirin (ASA) placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Aspirin (ASA) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Niacin extended-release (NER) placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Niacin extended-release (NER) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Humira (adalimumab) | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00761514 |
| Humira (adalimumab) | Other | Phase PHASE4 | Rheumatoid Arthritis | TERMINATED | NCT00761514 |
| medical food minus EPA and GLA, antioxidant vitamins/minerals | Other | Phase PHASE2 | Asthma | COMPLETED | NCT01087710 |
| medical food with EPA and GLA, vitamins and minerals | Other | Phase PHASE2 | Asthma | COMPLETED | NCT01087710 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| medical food minus EPA and GLA, antioxidant vitamins/minerals | Other | Phase PHASE2 | Asthma | COMPLETED | NCT01087710 |
| medical food with EPA and GLA, vitamins and minerals | Other | Phase PHASE2 | Asthma | COMPLETED | NCT01087710 |
| Ad lib diet; AN 777; exercise | Other | Phase PHASE2 | Aged | COMPLETED | NCT00798291 |
| Ad lib diet/ placebo/ exercise | Other | Phase PHASE2 | Aged | COMPLETED | NCT00798291 |
| Ad lib diet and An 777 | Other | Phase PHASE2 | Aged | COMPLETED | NCT00798291 |
| Ad lib diet and Control placebo | Other | Phase PHASE2 | Aged | COMPLETED | NCT00798291 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT00735787 |
| Placebo | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT00735787 |
| Increased dose of Kaletra | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT00414284 |
| Increased dose of Kaletra | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT00414284 |
| Ketoconazole | Other | Phase PHASE1 | Lymphoma | COMPLETED | NCT01021358 |
| ABT-263 | Other | Phase PHASE1 | Lymphoma | COMPLETED | NCT01021358 |
| Hydrocodone/Acetaminophen on Extended Release | Other | Phase PHASE3 | Moderate to Severe Chronic, Non-malignant Pain | COMPLETED | NCT00195728 |
| Zemplar Capsule | Other | Phase PHASE3 | Kidney Disease | COMPLETED | NCT00091975 |
| Zemplar Capsule | Other | Phase PHASE3 | Kidney Disease | COMPLETED | NCT00091975 |
| Zemplar Capsule | Other | Phase PHASE3 | Kidney Disease | COMPLETED | NCT00091975 |
| Clarithromycin | Other | Phase PHASE2 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000644 |
| Lupron (leuprolide acetate) | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00660010 |
| Lupron (leuprolide acetate) | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00660010 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Mitral Valve Repair Surgery | Procedure | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| MitraClip™ device implantation | Device | Approved | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04198870 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| Stopping nucleosides and continuing lopinavir/ritonavir monotherapy | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00114933 |
| sibutramine or placebo | Other | Phase PHASE3 | Obesity | TERMINATED | NCT00645255 |
| placebo | Other | Phase PHASE3 | Obesity | TERMINATED | NCT00645255 |
| sibutramine or placebo | Other | Phase PHASE3 | Obesity | TERMINATED | NCT00645255 |
| placebo | Other | Phase PHASE3 | Obesity | TERMINATED | NCT00645255 |
| cefdinir | Other | Phase PHASE2 | Acute Otitis Media | COMPLETED | NCT00645203 |
| cefdinir | Other | Phase PHASE2 | Acute Otitis Media | COMPLETED | NCT00645203 |
| cefdinir | Other | Phase PHASE2 | Acute Otitis Media | COMPLETED | NCT00645203 |
| amoxicillin | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00645125 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00645125 |
| amoxicillin | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00645125 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00645125 |
| azithromycin | Other | Phase PHASE4 | Acute Otitis Media | COMPLETED | NCT00645112 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Acute Otitis Media | COMPLETED | NCT00645112 |
| clarithromycin immediate-release tablets | Other | Phase PHASE3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | COMPLETED | NCT00645086 |
| clarithromycin extended-release tablets | Other | Phase PHASE3 | Acute Bacterial Exacerbation of Chronic Bronchitis (ABECB). | COMPLETED | NCT00645086 |
| levofloxacin | Other | Phase PHASE4 | Acute Bacterial Sinusitis | COMPLETED | NCT00645073 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Acute Bacterial Sinusitis | COMPLETED | NCT00645073 |
| amoxicillin | Other | Phase PHASE4 | Acute Otitis Media | COMPLETED | NCT00644943 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Acute Otitis Media | COMPLETED | NCT00644943 |
| amoxicillin | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644891 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644891 |
| azithromycin | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644774 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644774 |
| azithromycin | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644774 |
| cefdinir (Omnicef) | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00644774 |
| Depakote ER | Other | Phase PHASE2 | Pediatric Epilepsy | COMPLETED | NCT00646711 |
| Depakote Delayed-Release/Depakote Sprinkle | Other | Phase PHASE2 | Pediatric Epilepsy | COMPLETED | NCT00646711 |
| placebo for adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| placebo for adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| placebo for adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| adalimumab | Other | Phase PHASE2 | Arthritis | COMPLETED | NCT00646386 |
| adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00646191 |
| placebo for adalimumab | Other | Phase PHASE3 | Arthritis | COMPLETED | NCT00646178 |
| adalimumab | Other | Phase PHASE3 | Arthritis | COMPLETED | NCT00646178 |
| placebo for adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645905 |
| adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00645905 |
| placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00649922 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00649922 |
| placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647920 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647920 |
| Efavirenz | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038532 |
| Saquinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038532 |
| Amprenavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00038532 |
| lamivudine/zidovudine | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234923 |
| lopinavir/ritonavir | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234923 |
| Stavudine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| Lamivudine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| Lopinavir/Ritonavir | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| Stavudine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| Lamivudine | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| Lopinavir/Ritonavir | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00004578 |
| adalimumab | Other | Preclinical | Rheumatoid Arthritis | APPROVED_FOR_MARKETING | NCT00650026 |
| adalimumab | Other | Preclinical | Rheumatoid Arthritis | APPROVED_FOR_MARKETING | NCT00650026 |
| adalimumab | Other | Preclinical | Rheumatoid Arthritis | APPROVED_FOR_MARKETING | NCT00650026 |
| Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00427362 |
| Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT00427362 |
| Placebo | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| Sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| Placebo | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| Sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| Placebo | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| Sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00677391 |
| felodipine/ramipril | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| metoprolol/HCT | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| verapamil/trandolapril | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| felodipine/ramipril | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| metoprolol/HCT | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| verapamil/trandolapril | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| sibutramine | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00679653 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156156 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156156 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156156 |
| Placebo | Other | Phase PHASE2 | Leiomyoma | COMPLETED | NCT00160459 |
| Asoprisnil | Other | Phase PHASE2 | Leiomyoma | COMPLETED | NCT00160459 |
| Placebo | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160446 |
| Asoprisnil | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160446 |
| Placebo | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160433 |
| Asoprisnil | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160433 |
| Placebo | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160433 |
| Asoprisnil | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160433 |
| Asoprisnil | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160420 |
| Asoprisnil | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00160420 |
| Placebo | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00160381 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00160381 |
| Placebo | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00160381 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00160381 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156208 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156208 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00156208 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00156195 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00156195 |
| Asoprisnil/Premarin | Other | Phase PHASE2 | Postmenopause | COMPLETED | NCT00152295 |
| Placebo and Premarin | Other | Phase PHASE2 | Amenorrhea | COMPLETED | NCT00152282 |
| Asoprisnil/Premarin | Other | Phase PHASE2 | Amenorrhea | COMPLETED | NCT00152282 |
| Placebo and Premarin | Other | Phase PHASE2 | Amenorrhea | COMPLETED | NCT00152282 |
| Asoprisnil/Premarin | Other | Phase PHASE2 | Amenorrhea | COMPLETED | NCT00152282 |
| Placebo | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00152269 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00152269 |
| Placebo | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00152269 |
| Asoprisnil | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT00152269 |
| Placebo | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00152256 |
| Asoprisnil | Other | Phase PHASE3 | Fibroid Uterus | COMPLETED | NCT00152256 |
| Placebo | Other | Phase PHASE2 | Uterine Fibroids | COMPLETED | NCT00150644 |
| Asoprisnil | Other | Phase PHASE2 | Uterine Fibroids | COMPLETED | NCT00150644 |
| Milk based formula C | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| #3 Human Milk | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| #2 Standard formula | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| Milk based formula A | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| Milk based formula C | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| #3 Human Milk | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| #2 Standard formula | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| Milk based formula A | Other | Phase PHASE2 | Healthy | COMPLETED | NCT00543673 |
| Diabetes specific enteral product | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00520065 |
| enteral nutritional formula | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00520065 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235001 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235001 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235001 |
| lopinavir/ritonavir with 2 Nucleoside RTIs | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234910 |
| Tenofovir DF | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234910 |
| lopinavir/ritonavir with 2 Nucleoside RTIs | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234910 |
| Tenofovir DF | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT00234910 |
| verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| placebo | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| trandolapril | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| placebo | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| trandolapril | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00235014 |
| sibutramine hydochloride monohydrate | Other | Phase PHASE4 | Obesity | COMPLETED | NCT00234988 |
| sibutramine hydochloride monohydrate | Other | Phase PHASE4 | Obesity | COMPLETED | NCT00234988 |
| Lotrel (amlodipine/benazepril) | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234871 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234871 |
| Lotrel (amlodipine/benazepril) | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234871 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234871 |
| (Hyzaar) losartan/hydrochlorothiazide | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| (Hyzaar) losartan/hydrochlorothiazide | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| (Hyzaar) losartan/hydrochlorothiazide | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| trandolapril/verapamil | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00234858 |
| placebo adalimumab, placebo MTX | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00235820 |
| MTX | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00235820 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00235820 |
| Trandolapril | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00233532 |
| Trandolapril | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00233532 |
| Stenting: Renal Artery | Other | Phase PHASE3 | Renal Artery Obstruction | TERMINATED | NCT00180544 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00448383 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00448383 |
| Didanosine | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| Zidovudine | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| Clarithromycin | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| Didanosine | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| Zidovudine | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| Clarithromycin | Other | Phase PHASE1 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000971 |
| fenofibrate 160 mg and simvastatin 20 mg | Other | Approved | Type II Diabetes Mellitus | COMPLETED | NCT00309712 |
| simvastatin 20 mg and placebo | Other | Approved | Type II Diabetes Mellitus | COMPLETED | NCT00309712 |
| fenofibrate 160 mg and placebo | Other | Approved | Type II Diabetes Mellitus | COMPLETED | NCT00309712 |
| Divalproex | Other | Approved | Epilepsy | COMPLETED | NCT00347152 |
| Over-the-wire & Rapid Exchange ACCULINK (tm) Carotid Stent & ACCUNET (tm) embolic protection system | Other | Phase PHASE2 | Carotid Atherosclerosis | COMPLETED | NCT00180518 |
| Over-the-wire & Rapid Exchange ACCULINK (tm) Carotid Stent & ACCUNET (tm) embolic protection system | Other | Phase PHASE2 | Carotid Atherosclerosis | COMPLETED | NCT00180518 |
| Leuprolide acetate | Other | Approved | Prostatic Neoplasms | COMPLETED | NCT00056654 |
| Leuprolide acetate | Other | Approved | Prostatic Neoplasms | COMPLETED | NCT00056654 |
| Leuprolide acetate | Other | Approved | Prostatic Neoplasms | COMPLETED | NCT00056654 |
| Diabetes specific feeding product | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00544206 |
| standard enteral feeding product | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00544206 |
| Diabetes specific feeding product | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00544206 |
| standard enteral feeding product | Other | Phase PHASE2 | Type 2 Diabetes Mellitus | COMPLETED | NCT00544206 |
| TriMaxx Coronary Stent placement | Other | Phase PHASE1 | Coronary Artery Disease | COMPLETED | NCT00596661 |
| Carotid artery stenting with filter (interventional) | Other | Phase PHASE4 | Carotid Artery Disease | COMPLETED | NCT00287508 |
| Subunit influenza vaccine | Other | Phase PHASE4 | Immunosuppression | COMPLETED | NCT00783380 |
| Virosomal influenza vaccine | Other | Phase PHASE4 | Immunosuppression | COMPLETED | NCT00783380 |
| Subunit influenza vaccine | Other | Phase PHASE4 | Immunosuppression | COMPLETED | NCT00783380 |
| Virosomal influenza vaccine | Other | Phase PHASE4 | Immunosuppression | COMPLETED | NCT00783380 |
| Ensure Plus | Other | Phase PHASE4 | Esophageal Cancer | UNKNOWN | NCT00790140 |
| Prosure | Other | Phase PHASE4 | Esophageal Cancer | UNKNOWN | NCT00790140 |
| Ensure Plus | Other | Phase PHASE4 | Esophageal Cancer | UNKNOWN | NCT00790140 |
| Prosure | Other | Phase PHASE4 | Esophageal Cancer | UNKNOWN | NCT00790140 |
| Lopinavir/Ritonavir | Other | Phase PHASE4 | HIV Infection | TERMINATED | NCT00234962 |
| Lopinavir/Ritonavir | Other | Phase PHASE4 | HIV Infection | TERMINATED | NCT00234962 |
| Placebo | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00657774 |
| Oral Prednisone 10mg | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00657774 |
| FlutiForm 100/10 ug | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00657774 |
| FlutiForm 250/10 ug | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00657774 |
| milk protein formulas, varying carbohydrate/protein sources | Other | Phase PHASE2 | Infant, Newborn | COMPLETED | NCT00705562 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00269386 |
| Clarithromycin | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00269386 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00269386 |
| Clarithromycin | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00269386 |
| adalimumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00827996 |
| adalimumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00827996 |
| Multilink Vision™ Stent (CE-labeled) | Other | Preclinical | Coronary Disease | COMPLETED | NCT00243438 |
| Multilink Vision™ Stent (CE-labeled) | Other | Preclinical | Coronary Disease | COMPLETED | NCT00243438 |
| Multilink Vision™ Stent (CE-labeled) | Other | Preclinical | Coronary Disease | COMPLETED | NCT00243438 |
| Valproic Acid and Depakote ER | Other | Phase PHASE4 | Mood Disorder | COMPLETED | NCT00211250 |
| Valproic Acid and Depakote ER | Other | Phase PHASE4 | Mood Disorder | COMPLETED | NCT00211250 |
| Valproic Acid and Depakote ER | Other | Phase PHASE4 | Mood Disorder | COMPLETED | NCT00211250 |
| placebo | Other | Phase PHASE4 | Venous Insufficiency | COMPLETED | NCT00835822 |
| Venocur Triplex® | Other | Phase PHASE4 | Venous Insufficiency | COMPLETED | NCT00835822 |
| placebo | Other | Phase PHASE4 | Venous Insufficiency | COMPLETED | NCT00835822 |
| Venocur Triplex® | Other | Phase PHASE4 | Venous Insufficiency | COMPLETED | NCT00835822 |
| NUCS | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| Ribavirin | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| PEG-IFNa 2a | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| LPV/r | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| NUCS | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| Ribavirin | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| PEG-IFNa 2a | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| LPV/r | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437684 |
| Ribavirin | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| PEG-IFNa 2a | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| Nucleoside Reverse Transcriptase Inhibitors | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| LPV/r | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| Ribavirin | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| PEG-IFNa 2a | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| Nucleoside Reverse Transcriptase Inhibitors | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| LPV/r | Other | Phase PHASE3 | HIV Infections | UNKNOWN | NCT00437476 |
| lopinavir/ritonavir | Other | Phase PHASE4 | HIV Infection | TERMINATED | NCT00420355 |
| atazanavir | Other | Phase PHASE4 | HIV Infection | TERMINATED | NCT00420355 |
| Anti-HIV Immune Serum Globulin (Human) | Other | Phase PHASE1 | HIV Infections | COMPLETED | NCT00002036 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 20% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Fat Emulsion 2% | Other | Approved | HIV Infections | COMPLETED | NCT00002029 |
| Asoprisnil | Other | Phase PHASE2 | Leiomyoma | COMPLETED | NCT00156182 |
| Asoprisnil | Other | Phase PHASE2 | Leiomyoma | COMPLETED | NCT00156182 |
| Diabetes Meal Plan with experimental diabetes-specific nutritional shake, diabetes specific cereal, and diabetes specific snack bars. | Other | Phase PHASE3 | Diabetes Mellitus, Type 2 | COMPLETED | NCT00753181 |
| Usual diet | Other | Phase PHASE3 | Diabetes Mellitus, Type 2 | COMPLETED | NCT00753181 |
| Nutritional Formula | Other | Phase PHASE3 | Diabetes Mellitus, Type 2 | COMPLETED | NCT00753181 |
| Preterm infant formula with added soluble lipids | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT00707837 |
| Preterm infant formulas and discharge formulas | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT00707837 |
| Preterm infant formula with added soluble lipids | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT00707837 |
| Preterm infant formulas and discharge formulas | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT00707837 |
| paricalcitol | Other | Phase PHASE2 | End Stage Renal Disease | COMPLETED | NCT00686751 |
| Medical antitrhombotic treatment | Drug | Phase PHASE4 | Embolism, Paradoxical | UNKNOWN | NCT00166257 |
| Percutaneous closure of patent foramen ovale | Other | Phase PHASE4 | Embolism, Paradoxical | UNKNOWN | NCT00166257 |
| Placebo | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| paricalcitol | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| Placebo | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| paricalcitol | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| Placebo | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| paricalcitol | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00428246 |
| Placebo | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00300469 |
| Atorvastatin | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00300469 |
| ABT-335 | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00300469 |
| Placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| Simvastatin | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| Placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| Simvastatin | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300456 |
| Placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| Rosuvastatin Calcium | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| Placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| Rosuvastatin Calcium | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| Placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| Rosuvastatin Calcium | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300482 |
| FreeStyle Navigator Continuous Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT00920881 |
| ezetimibe | Other | Phase PHASE4 | Atherosclerosis | TERMINATED | NCT00397657 |
| extended release niacin | Other | Phase PHASE4 | Atherosclerosis | TERMINATED | NCT00397657 |
| ezetimibe | Other | Phase PHASE4 | Atherosclerosis | TERMINATED | NCT00397657 |
| extended release niacin | Other | Phase PHASE4 | Atherosclerosis | TERMINATED | NCT00397657 |
| ABT-335 and simvastatin | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300430 |
| ABT-335 and atorvastatin calcium | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300430 |
| ABT-335 and rosuvastatin calcium | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00300430 |
| Alendronate | Other | Phase PHASE3 | Osteoporosis | TERMINATED | NCT00236002 |
| Alendronate | Other | Phase PHASE3 | Osteoporosis | TERMINATED | NCT00236002 |
| Different insulin therapy at different time points | Drug | Approved | Type 1 Diabetes | COMPLETED | NCT00970567 |
| Different insulin therapy at different time points | Drug | Approved | Type 1 Diabetes | COMPLETED | NCT00970567 |
| aspirin placebo (ASA Pbo) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| aspirin (ASA) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| niacin extended-release (NER) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| aspirin placebo (ASA Pbo) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| aspirin (ASA) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| niacin extended-release (NER) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00626392 |
| divalproex sodium extended release | Other | Phase PHASE2 | Alcoholism | COMPLETED | NCT00202514 |
| divalproex sodium extended release | Other | Phase PHASE2 | Alcoholism | COMPLETED | NCT00202514 |
| Aspirin (ASA) placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Aspirin (ASA) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Niacin extended-release (NER) placebo | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| Niacin extended-release (NER) | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT00630877 |
| MEMS cap | Other | Preclinical | HIV Infection | COMPLETED | NCT00200369 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00427921 |
| Biomarkers | Other | Preclinical | Acute Coronary Syndrome (ACS) | COMPLETED | NCT00415948 |
| Hectorol® injection | Other | Phase PHASE4 | Chronic Kidney Disease, Stage 5 | COMPLETED | NCT00257920 |
| Zemplar® injection | Other | Phase PHASE4 | Chronic Kidney Disease, Stage 5 | COMPLETED | NCT00257920 |
| Hectorol® injection | Other | Phase PHASE4 | Chronic Kidney Disease, Stage 5 | COMPLETED | NCT00257920 |
| Zemplar® injection | Other | Phase PHASE4 | Chronic Kidney Disease, Stage 5 | COMPLETED | NCT00257920 |
| Standard ICU enteral diet, isocaloric to the study diet | Other | Phase PHASE4 | Sepsis | COMPLETED | NCT00329680 |
| Eicosapentaenoic acid, Gamma-Linolenic Acid and Antioxidant Vitamins | Other | Phase PHASE4 | Sepsis | COMPLETED | NCT00329680 |
| Standard ICU enteral diet, isocaloric to the study diet | Other | Phase PHASE4 | Sepsis | COMPLETED | NCT00329680 |
| Eicosapentaenoic acid, Gamma-Linolenic Acid and Antioxidant Vitamins | Other | Phase PHASE4 | Sepsis | COMPLETED | NCT00329680 |
| Coronary artery stent placement | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00180453 |
| Coronary artery drug eluting stent placement | Drug | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00180453 |
| EPA-DHA arm | Other | Phase PHASE2 | Lung Cancer | UNKNOWN | NCT01048970 |
| Nutritional Assessment | Other | Phase PHASE2 | Lung Cancer | UNKNOWN | NCT01048970 |
| EPA-DHA arm | Other | Phase PHASE2 | Lung Cancer | UNKNOWN | NCT01048970 |
| Nutritional Assessment | Other | Phase PHASE2 | Lung Cancer | UNKNOWN | NCT01048970 |
| iSTAT point of care analyzer | Other | Phase PHASE4 | Unstable Angina | COMPLETED | NCT00276432 |
| iSTAT point of care analyzer | Other | Phase PHASE4 | Unstable Angina | COMPLETED | NCT00276432 |
| Lithium | Other | Phase PHASE4 | Bipolar Disorder | WITHDRAWN | NCT01075126 |
| Depakote | Other | Phase PHASE4 | Bipolar Disorder | WITHDRAWN | NCT01075126 |
| Lithium | Other | Phase PHASE4 | Bipolar Disorder | WITHDRAWN | NCT01075126 |
| Depakote | Other | Phase PHASE4 | Bipolar Disorder | WITHDRAWN | NCT01075126 |
| ABSOLUTE™: Self-Expandable Peripheral Nitinol Stent | Other | Phase PHASE4 | Peripheral Vascular Diseases | COMPLETED | NCT00180505 |
| ABT-263 | Other | Phase PHASE2 | B-cell Chronic Lymphocytic Leukemia | WITHDRAWN | NCT00918450 |
| ABT-263 | Other | Phase PHASE2 | B-cell Chronic Lymphocytic Leukemia | WITHDRAWN | NCT00918450 |
| ABT-263 | Other | Phase PHASE2 | B-cell Chronic Lymphocytic Leukemia | WITHDRAWN | NCT00918450 |
| Niacin and aspirin | Other | Preclinical | Flushing | COMPLETED | NCT00930839 |
| Paricalcitol | Other | Phase PHASE4 | Kidney Failure | COMPLETED | NCT00294866 |
| Standard physician-directed weaning | Other | Phase PHASE3 | Respiratory Insufficiency | COMPLETED | NCT00473148 |
| BNP-guided weaning | Other | Phase PHASE3 | Respiratory Insufficiency | COMPLETED | NCT00473148 |
| Standard physician-directed weaning | Other | Phase PHASE3 | Respiratory Insufficiency | COMPLETED | NCT00473148 |
| BNP-guided weaning | Other | Phase PHASE3 | Respiratory Insufficiency | COMPLETED | NCT00473148 |
| Matched placebo | Other | Phase PHASE2 | Hodgkin Disease | TERMINATED | NCT00275262 |
| Leuprolide acetate depot (LAD) 11.25 mg 3 Month | Other | Phase PHASE2 | Hodgkin Disease | TERMINATED | NCT00275262 |
| Matched placebo | Other | Phase PHASE2 | Hodgkin Disease | TERMINATED | NCT00275262 |
| Leuprolide acetate depot (LAD) 11.25 mg 3 Month | Other | Phase PHASE2 | Hodgkin Disease | TERMINATED | NCT00275262 |
| Zoledronic Acid (Zometa) | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00181558 |
| Atrasentan | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00181558 |
| Zoledronic Acid (Zometa) | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00181558 |
| Atrasentan | Other | Phase PHASE2 | Prostate Cancer | COMPLETED | NCT00181558 |
| Placebo | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00234832 |
| Sibutramine hydrochloride | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00234832 |
| Placebo | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00234832 |
| Sibutramine hydrochloride | Other | Phase PHASE3 | Obesity | COMPLETED | NCT00234832 |
| Sampling Rate | Other | Preclinical | Healthy | COMPLETED | NCT01126567 |
| Sampling Rate | Other | Preclinical | Healthy | COMPLETED | NCT01126567 |
| Placebo | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Divalproex | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Placebo | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Divalproex | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Placebo | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Divalproex | Other | Phase PHASE3 | Bipolar Spectrum Disorder With Moderate-to- Severe Hypomania or Mild Mania | COMPLETED | NCT00278772 |
| Treatment with Adalimumab | Drug | Approved | Crohn's Disease | UNKNOWN | NCT01144156 |
| Treatment with Adalimumab | Drug | Approved | Crohn's Disease | UNKNOWN | NCT01144156 |
| Treatment with Adalimumab | Drug | Approved | Crohn's Disease | UNKNOWN | NCT01144156 |
| herbal extract; root of woody shrub grown in India/Sri-Lanka | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00499148 |
| herbal extract; root of woody shrub grown in India/Sri-Lanka | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00499148 |
| Endorectal Coil Magnetic Resonance Images | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00160953 |
| Endorectal Coil Magnetic Resonance Images | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00160953 |
| Endorectal Coil Magnetic Resonance Images | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00160953 |
| Endorectal Coil Magnetic Resonance Images | Other | Phase PHASE2 | Prostatic Neoplasms | COMPLETED | NCT00160953 |
| Standard food | Other | Phase PHASE3 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01188200 |
| Experimental nutritional formula #M979 | Other | Phase PHASE3 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01188200 |
| fluticasone propionate, formoterol fumarate | Other | Phase PHASE2 | Mild to Moderate Asthma | COMPLETED | NCT00734292 |
| fluticasone propionate, formoterol fumarate | Other | Phase PHASE2 | Mild to Moderate Asthma | COMPLETED | NCT00734292 |
| fluticasone propionate, formoterol fumarate | Other | Phase PHASE2 | Mild to Moderate Asthma | COMPLETED | NCT00734292 |
| Flovent Fluticasone HFA | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| SKP-Fluticasone | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| FlutiForm 250/10 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| Flovent Fluticasone HFA | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| SKP-Fluticasone | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| FlutiForm 250/10 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00649025 |
| ABT-263 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00743028 |
| ABT-263 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00743028 |
| Placebo for ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| Placebo for ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| Placebo for ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| Placebo for ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00931281 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909636 |
| ABT-333 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909636 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909636 |
| ABT-333 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909636 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909311 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909311 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909311 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00909311 |
| ABT-333 Capsule | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| ABT-333 Tablet | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| ABT-333 Capsule | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| ABT-333 Tablet | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00895102 |
| placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| ketoconazole | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| ABT-333 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| ketoconazole | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| ABT-333 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00768690 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Phase PHASE4 | Coronary Disease | COMPLETED | NCT00402272 |
| ABT-335 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00839293 |
| ABT-335 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00839293 |
| ABT-335 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00839293 |
| Ezetimibe | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Atorvastatin | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| ABT-335 | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Ezetimibe | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Atorvastatin | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| ABT-335 | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Ezetimibe | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Atorvastatin | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| ABT-335 | Other | Phase PHASE1 | Pharmacokinetics | COMPLETED | NCT00681525 |
| Placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00982826 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00982826 |
| Placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00982826 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00982826 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00947440 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00947440 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00890318 |
| ketoconazole | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00890318 |
| ABT-072 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00890318 |
| placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00752687 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00752687 |
| placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00752687 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT00752687 |
| Placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| Placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| Placebo | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| ABT-072 | Other | Phase PHASE1 | Hepatitis C | COMPLETED | NCT01081483 |
| Placebo | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| ABT-333 | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| Placebo | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| ABT-333 | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| Placebo | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| ABT-333 | Other | Phase PHASE1 | HCV Infections | COMPLETED | NCT00919490 |
| Placebo for ABT-126 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT01043458 |
| ABT-126 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT01043458 |
| Placebo for ABT-126 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT01043458 |
| ABT-126 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT01043458 |
| ABT-614 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00959816 |
| ABT-614 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00959816 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00912431 |
| ABT-126 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00912431 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00912431 |
| ABT-126 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00912431 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT00867399 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT00867399 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00854659 |
| ABT-102 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00854659 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00854659 |
| ABT-102 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00854659 |
| ABT-614 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00788801 |
| rifabutin | Other | Phase PHASE1 | HIV | TERMINATED | NCT00743470 |
| lopinavir/ritonavir | Other | Phase PHASE1 | HIV | TERMINATED | NCT00743470 |
| rifabutin | Other | Phase PHASE1 | HIV | TERMINATED | NCT00743470 |
| lopinavir/ritonavir | Other | Phase PHASE1 | HIV | TERMINATED | NCT00743470 |
| placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| atomoxetine | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| ABT-894 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| atomoxetine | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| ABT-894 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| atomoxetine | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| ABT-894 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00429091 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| ABT-436 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| ABT-436 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| ABT-436 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01050127 |
| Matching placebo to ABT-384 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00968422 |
| ABT-384 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00968422 |
| Matching placebo to ABT-384 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00968422 |
| ABT-384 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00968422 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00959634 |
| ABT-126 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00959634 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00959634 |
| ABT-126 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00959634 |
| ABT-874 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870948 |
| ABT-874 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870948 |
| ABT-874 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870948 |
| ABT-263 | Other | Phase PHASE1 | Healthy Female Subjects | COMPLETED | NCT01053520 |
| ABT-263 | Other | Phase PHASE1 | Healthy Female Subjects | COMPLETED | NCT01053520 |
| Human Milk | Other | Phase PHASE3 | Healthy Term Infants | TERMINATED | NCT01137877 |
| Investigational Infant Formula #2 | Other | Phase PHASE3 | Healthy Term Infants | TERMINATED | NCT01137877 |
| Investigational Infant Formula #1 | Other | Phase PHASE3 | Healthy Term Infants | TERMINATED | NCT01137877 |
| Milk based infant formula powder | Other | Phase PHASE3 | Healthy Term Infants | TERMINATED | NCT01137877 |
| Experimental milk protein infant formula Process F | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Experimental milk protein infant formula Process E | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Experimental milk protein infant formula Process D | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Experimental milk protein infant formula Process C | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Experimental milk protein infant formula Process B | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Experimental milk protein infant formula Process A | Other | Phase PHASE3 | Gastrointestinal Tolerance | COMPLETED | NCT00977964 |
| Glucose drink | Other | Phase PHASE2 | Overweight | COMPLETED | NCT00974831 |
| Amino Acid Drink Mixture | Other | Phase PHASE2 | Overweight | COMPLETED | NCT00974831 |
| Infant formula milk based | Other | Phase PHASE4 | Infant | COMPLETED | NCT00941564 |
| Infant Formula milk based | Other | Phase PHASE4 | Infant | COMPLETED | NCT00941564 |
| ABT-384 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01009216 |
| ritonavir | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01091649 |
| ABT-450 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01091649 |
| ritonavir | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01091649 |
| ABT-450 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01091649 |
| EES vs. SES | Other | Approved | Ischemic Heart Disease | UNKNOWN | NCT01266239 |
| kissing balloon inflation | Other | Approved | Ischemic Heart Disease | UNKNOWN | NCT01266239 |
| EES vs. SES | Other | Approved | Ischemic Heart Disease | UNKNOWN | NCT01266239 |
| kissing balloon inflation | Other | Approved | Ischemic Heart Disease | UNKNOWN | NCT01266239 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01270087 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01270087 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01270087 |
| Docetaxel | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| Placebo | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| ABT-751 | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| Docetaxel | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| Placebo | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| ABT-751 | Other | Phase PHASE1 | Lung Cancer | TERMINATED | NCT00354562 |
| Tarceva | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| Tarceva | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| Tarceva | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | WITHDRAWN | NCT00754104 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404391 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404183 |
| Extended-Release Hydrocodone/Acetaminophen | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404183 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404183 |
| Extended-Release Hydrocodone/Acetaminophen | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404183 |
| Hydrocodone/Acetaminophen on Extended Release | Other | Phase PHASE3 | Moderate to Severe Chronic, Non-malignant Pain | COMPLETED | NCT00195728 |
| Placebo | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Hydrocodone/Acetaminophen Extended-Release | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Placebo | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Hydrocodone/Acetaminophen Extended-Release | Other | Phase PHASE3 | Pain | COMPLETED | NCT00402792 |
| Placebo | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00298974 |
| hydrocodone / acetaminophen extended release | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00298974 |
| Placebo | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00298974 |
| hydrocodone / acetaminophen extended release | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00298974 |
| atrasentan hydrochloride | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00046943 |
| atrasentan hydrochloride | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00046943 |
| atrasentan hydrochloride | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00046943 |
| Clarithromycin | Other | Phase PHASE2 | Mycobacterium Avium-intracellulare Infection | COMPLETED | NCT00000644 |
| Dynalink®-E, everolimus-eluting peripheral stent | Other | Approved | Atherosclerosis | COMPLETED | NCT00475566 |
| Dynalink®-E everolimus-eluting peripheral stent | Other | Approved | Atherosclerosis | COMPLETED | NCT00475566 |
| Ergocalciferol | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00958451 |
| Paricalcitol | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00958451 |
| Placebo comparator | Other | Phase PHASE1 | Aged | COMPLETED | NCT00945581 |
| Experimental Nutritional Powder Formula | Other | Phase PHASE1 | Aged | COMPLETED | NCT00945581 |
| Placebo comparator | Other | Phase PHASE1 | Aged | COMPLETED | NCT00945581 |
| Experimental Nutritional Powder Formula | Other | Phase PHASE1 | Aged | COMPLETED | NCT00945581 |
| #3 Nutritional ingredient + Fiber | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01326299 |
| #2 Nutritional ingredient + Fiber | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01326299 |
| #1 Nutritional ingredient +Fiber | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01326299 |
| Nutritional ingredient | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01326299 |
| Carbohydrate placebo | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01326299 |
| 10004RF | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01324921 |
| Breakfast | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01324921 |
| No breakfast/beverage only | Other | Phase PHASE2 | Diabetes Mellitus, Type 2 | COMPLETED | NCT01324921 |
| TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent System | Other | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00148356 |
| ZoMaxx™ Drug-Eluting Coronary Stent System | Drug | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00148356 |
| TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent System | Other | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00148356 |
| ZoMaxx™ Drug-Eluting Coronary Stent System | Drug | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00148356 |
| clarithromycin (Klacid) granules for oral suspension | Other | Preclinical | Lower Respiratory Tract Infection | COMPLETED | NCT01076166 |
| clarithromycin (Klacid) granules for oral suspension | Other | Preclinical | Lower Respiratory Tract Infection | COMPLETED | NCT01076166 |
| Adalimumab 40 mg eow or ew | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT01070303 |
| Adalimumab 40 mg eow or ew | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT01070303 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00647270 |
| Adalimumab 40 mg | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT00538902 |
| Adalimumab 80 mg | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT00538902 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT00538902 |
| Humira (adalimumab) | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00513370 |
| Humira (adalimumab) | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00513370 |
| Humira (adalimumab) | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00513370 |
| placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00385736 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00385736 |
| lopinavir/ritonavir (LPV/r) tablet with nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infections | COMPLETED | NCT00358917 |
| lopinavir/ritonavir (LPV/r) tablet with nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infections | COMPLETED | NCT00358917 |
| lopinavir/ritonavir (LPV/r) tablet with nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infections | COMPLETED | NCT00358917 |
| placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00348283 |
| OL adalimumab 40 mg | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| DB adalimumab 40 mg ew | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| DB adalimumab 40 mg eow | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| Double-blind (DB) adalimumab placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| OL adalimumab 40 mg | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| DB adalimumab 40 mg ew | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| DB adalimumab 40 mg eow | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| Double-blind (DB) adalimumab placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00055497 |
| Lupron (leuprolide acetate) | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00660010 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00566722 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00566722 |
| placebo (vehicle ointment) | Other | Phase PHASE3 | Chronic Plaque Psoriasis | COMPLETED | NCT00574249 |
| Calcipotriol/Betamethasone Ointment | Other | Phase PHASE3 | Chronic Plaque Psoriasis | COMPLETED | NCT00574249 |
| adalimumab | Other | Phase PHASE3 | Chronic Plaque Psoriasis | COMPLETED | NCT00574249 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00195676 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00195676 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT00195676 |
| Paricalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00701805 |
| Paricalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00701805 |
| Paricalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00701805 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| adalimumab (D2E7) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| adalimumab (D2E7) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| adalimumab (D2E7) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00085644 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT01231321 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT01231321 |
| adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT01231321 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT00412620 |
| ABT-925 | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT00412620 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT00412620 |
| ABT-925 | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT00412620 |
| placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00408629 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00408629 |
| placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00408629 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00408629 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00918255 |
| adalimumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00918255 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00918255 |
| adalimumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT00918255 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00195819 |
| adalimumab (D2E7) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00195819 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00555204 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00555204 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | TERMINATED | NCT00554385 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | TERMINATED | NCT00554385 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | TERMINATED | NCT00554385 |
| SLV337 capsule | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01176201 |
| SLV337 suspension | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01176201 |
| SLV337 capsule | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01176201 |
| SLV337 suspension | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01176201 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT01146015 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT01146015 |
| Influenza Vaccine | Other | Phase PHASE3 | Influenza | COMPLETED | NCT00999206 |
| Influenza Vaccine | Other | Phase PHASE3 | Influenza | COMPLETED | NCT00999206 |
| pramipexole | Other | Phase PHASE2 | Advanced Stage Parkinson's Disease | TERMINATED | NCT00903838 |
| pardoprunox | Other | Phase PHASE2 | Advanced Stage Parkinson's Disease | TERMINATED | NCT00903838 |
| pramipexole | Other | Phase PHASE2 | Advanced Stage Parkinson's Disease | TERMINATED | NCT00903838 |
| pardoprunox | Other | Phase PHASE2 | Advanced Stage Parkinson's Disease | TERMINATED | NCT00903838 |
| AndroGel (testosterone gel) 1% | Other | Preclinical | Hypogonadism | COMPLETED | NCT01143818 |
| AndroGel (testosterone gel) 1% | Other | Preclinical | Hypogonadism | COMPLETED | NCT01143818 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Placebo | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT00941746 |
| PG110 | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT00941746 |
| Placebo | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT00941746 |
| PG110 | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT00941746 |
| ezetimibe | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| atorvastatin | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| placebo | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| ezetimibe | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| atorvastatin | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| placebo | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| ABT-335 | Other | Phase PHASE3 | Dyslipidemias | COMPLETED | NCT00639158 |
| atorvastatin | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| Niacin ER/Simvastatin Tablets | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| atorvastatin | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| Niacin ER/Simvastatin Tablets | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| atorvastatin | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| Niacin ER/Simvastatin Tablets | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT00465088 |
| SKP FlutiForm HFA pMDI | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00747318 |
| SKP FlutiForm HFA pMDI | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00747318 |
| SKP FlutiForm HFA pMDI | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00747318 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00195819 |
| adalimumab (D2E7) | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT00195819 |
| Placebo | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| ABT-652 | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| Placebo | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| ABT-652 | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| Placebo | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| ABT-652 | Other | Phase PHASE1 | Sleep Disorder | COMPLETED | NCT01124851 |
| Clarithromycin (Klacid SR) | Other | Preclinical | Respiratory Tract Infections | COMPLETED | NCT01095978 |
| Clarithromycin (Klacid SR) | Other | Preclinical | Respiratory Tract Infections | COMPLETED | NCT01095978 |
| maxacalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00990704 |
| paricalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00990704 |
| maxacalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00990704 |
| paricalcitol | Other | Phase PHASE2 | Secondary Hyperparathyroidism | COMPLETED | NCT00990704 |
| Clarithromycin (Klacid® MR) | Other | Preclinical | Respiratory Tract Infection | COMPLETED | NCT01076153 |
| Clarithromycin (Klacid® MR) | Other | Preclinical | Respiratory Tract Infection | COMPLETED | NCT01076153 |
| Clarithromycin (Klacid® MR) | Other | Preclinical | Respiratory Tract Infection | COMPLETED | NCT01076153 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00195715 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00195715 |
| fMRI | Other | Preclinical | Pathological Gambling | TERMINATED | NCT00211822 |
| fMRI | Other | Preclinical | Pathological Gambling | TERMINATED | NCT00211822 |
| Depacon IV and Depakote ER | Other | Approved | Cluster Headache | COMPLETED | NCT00203242 |
| Depacon IV and Depakote ER | Other | Approved | Cluster Headache | COMPLETED | NCT00203242 |
| palivizumab | Other | Phase PHASE2 | Respiratory Syncytial Virus Infection | COMPLETED | NCT01006629 |
| palivizumab | Other | Phase PHASE2 | Respiratory Syncytial Virus Infection | COMPLETED | NCT01006629 |
| palivizumab | Other | Phase PHASE2 | Respiratory Syncytial Virus Infection | COMPLETED | NCT01006629 |
| Leuprolide acetate - Formulation B | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00626431 |
| Leuprolide acetate - Formulation A | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00626431 |
| Leuprolide acetate - Formulation B | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00626431 |
| Leuprolide acetate - Formulation A | Other | Phase PHASE3 | Prostate Cancer | COMPLETED | NCT00626431 |
| lopinavir/ritonavir and raltegravir | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00752037 |
| lopinavir/ritonavir and raltegravir | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00752037 |
| lopinavir/ritonavir and raltegravir | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00752037 |
| TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent | Other | Phase PHASE3 | Coronary Disease | COMPLETED | NCT00180310 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Phase PHASE3 | Coronary Disease | COMPLETED | NCT00180310 |
| CRT off | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00900549 |
| CRT on | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00900549 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| Hydrocodone/Acetaminophen Immediate Release (NORCO®) | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| Hydrocodone/Acetaminophen Extended-Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| Hydrocodone/Acetaminophen Immediate Release (NORCO®) | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| Hydrocodone/Acetaminophen Extended-Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00404222 |
| placebo | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| hydrocodone/acetaminophen extended release (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| Extended release hydrocodone and acetaminophen (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| placebo | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| hydrocodone/acetaminophen extended release (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| Extended release hydrocodone and acetaminophen (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| placebo | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| hydrocodone/acetaminophen extended release (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| Extended release hydrocodone and acetaminophen (Vicodin CR) | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00325949 |
| ketoconazole | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| ketoconazole | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| ketoconazole | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01114191 |
| discharge vs. overnight stay | Other | Preclinical | Cardiovascular Disease | COMPLETED | NCT01230606 |
| discharge vs. overnight stay | Other | Preclinical | Cardiovascular Disease | COMPLETED | NCT01230606 |
| Placebo | Other | Phase PHASE3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | COMPLETED | NCT00400842 |
| SA-001 | Other | Phase PHASE3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | COMPLETED | NCT00400842 |
| Placebo | Other | Phase PHASE3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | COMPLETED | NCT00400842 |
| SA-001 | Other | Phase PHASE3 | Exocrine Pancreatic Insufficiency, Chronic Pancreatitis | COMPLETED | NCT00400842 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | UNKNOWN | NCT01405326 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | UNKNOWN | NCT01405326 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | UNKNOWN | NCT01405326 |
| Placebo | Other | Phase PHASE3 | Steatorrhea | TERMINATED | NCT00623025 |
| Creon 25000 | Other | Phase PHASE3 | Steatorrhea | TERMINATED | NCT00623025 |
| Placebo | Other | Phase PHASE3 | Steatorrhea | TERMINATED | NCT00623025 |
| Creon 25000 | Other | Phase PHASE3 | Steatorrhea | TERMINATED | NCT00623025 |
| SA-001 | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | COMPLETED | NCT00401076 |
| SA-001 | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency, Chronic Pancreatitis, Pancreatectomy | COMPLETED | NCT00401076 |
| Lopinavir/ritonavir (Kaletra) | Other | Preclinical | HIV-1 Infections | COMPLETED | NCT01074931 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00409682 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00409682 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01083810 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01083810 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01083810 |
| OLE FD Adalimumab +/- MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| OLE BSA Adalimumab +/- MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| Double-Blind Adalimumab/Placebo | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| Double-Blind Adalimumab/Placebo + MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| OLE FD Adalimumab +/- MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| OLE BSA Adalimumab +/- MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| Double-Blind Adalimumab/Placebo | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| Double-Blind Adalimumab/Placebo + MTX | Other | Phase PHASE3 | Arthritis, Juvenile Idiopathic | COMPLETED | NCT00048542 |
| ABT-874 | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT00562887 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT00562887 |
| ABT-874 | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT00562887 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT00562887 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00555204 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00555204 |
| placebo | Other | Phase PHASE1 | Pharmacokinetics | TERMINATED | NCT00985478 |
| SLV342 | Other | Phase PHASE1 | Pharmacokinetics | TERMINATED | NCT00985478 |
| placebo | Other | Phase PHASE1 | Pharmacokinetics | TERMINATED | NCT00985478 |
| SLV342 | Other | Phase PHASE1 | Pharmacokinetics | TERMINATED | NCT00985478 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT00881842 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT00881842 |
| Placebo | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00683176 |
| Choline Fenofibrate | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00683176 |
| Placebo | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00683176 |
| Choline Fenofibrate | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00683176 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195702 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195702 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195702 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195702 |
| Placebo | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Dydrogesterone | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Placebo | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Dydrogesterone | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Placebo | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Dydrogesterone | Other | Phase PHASE3 | Recurrent Miscarriage | COMPLETED | NCT00193674 |
| Placebo capsules | Other | Phase PHASE1 | Cognition Disorders | TERMINATED | NCT01133574 |
| SLV354 capsules | Other | Phase PHASE1 | Cognition Disorders | TERMINATED | NCT01133574 |
| Placebo capsules | Other | Phase PHASE1 | Cognition Disorders | TERMINATED | NCT01133574 |
| SLV354 capsules | Other | Phase PHASE1 | Cognition Disorders | TERMINATED | NCT01133574 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00809510 |
| ABT-089 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT00809510 |
| Adalimumab Every Week | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT00927069 |
| Adalimumab every other week | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT00927069 |
| Bioabsorbable Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Disease | COMPLETED | NCT00300131 |
| Bioabsorbable Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Disease | COMPLETED | NCT00300131 |
| Atenolol/HCTZ/Trandolapril | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00133692 |
| Verapamil SR/Trandolapril/Hydrochlorothiazide (HCTZ) | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00133692 |
| Zemplar iv (paricalcitol iv) | Other | Preclinical | Parathyroid Hormone | COMPLETED | NCT01084538 |
| Zemplar iv (paricalcitol iv) | Other | Preclinical | Parathyroid Hormone | COMPLETED | NCT01084538 |
| Placebo | Other | Phase PHASE2 | Traumatic Brain Injury | TERMINATED | NCT00735085 |
| SLV334 | Other | Phase PHASE2 | Traumatic Brain Injury | TERMINATED | NCT00735085 |
| Placebo | Other | Phase PHASE2 | Traumatic Brain Injury | TERMINATED | NCT00735085 |
| SLV334 | Other | Phase PHASE2 | Traumatic Brain Injury | TERMINATED | NCT00735085 |
| adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT00234884 |
| adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT00234884 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00409617 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00409617 |
| Placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00391729 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00391729 |
| Placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00391729 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00391729 |
| briakinumab | Other | Phase PHASE1 | Moderate to Severe Plaque Psoriasis | WITHDRAWN | NCT01260844 |
| Raltegravir; valproic acid | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00614458 |
| Raltegravir; valproic acid | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00614458 |
| Paricalcitol capsules | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00537979 |
| Paricalcitol injection | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00537979 |
| Influenza Vaccine | Other | Phase PHASE2 | Influenza Vaccines | COMPLETED | NCT01013675 |
| Influenza Vaccine | Other | Phase PHASE2 | Influenza Vaccines | COMPLETED | NCT01013675 |
| Placebo | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01181570 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01181570 |
| adalimumab (HUMIRA®) | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01078571 |
| Topical treatment | Drug | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| UVB Phototherapy | Drug | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| Topical treatment | Drug | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| UVB Phototherapy | Drug | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT00940862 |
| Zemplar (paricalcitol) | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00891813 |
| Zemplar (paricalcitol) | Other | Phase PHASE4 | Secondary Hyperparathyroidism | COMPLETED | NCT00891813 |
| Investigational Infant Formula B | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Investigational Infant Formula A | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Hydrolysate based infant formula | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Investigational Infant Formula B | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Investigational Infant Formula A | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Hydrolysate based infant formula | Other | Phase PHASE3 | Healthy Term Infants | COMPLETED | NCT01155414 |
| Rifampin | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01401933 |
| Linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01401933 |
| Rifampin | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01401933 |
| Linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01401933 |
| Drink mix calorically similar to experimental product | Other | Phase PHASE3 | Foot Ulcer, Diabetic | COMPLETED | NCT00711217 |
| Medical Food | Other | Phase PHASE3 | Foot Ulcer, Diabetic | COMPLETED | NCT00711217 |
| Leuprolide acetate 30 mg | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00635817 |
| Leuprolide acetate 11.25 mg | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00635817 |
| Leuprolide acetate 30 mg | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00635817 |
| Leuprolide acetate 11.25 mg | Other | Phase PHASE3 | Puberty, Precocious | COMPLETED | NCT00635817 |
| placebo | Other | Phase PHASE1 | Hypogonadal Males | COMPLETED | NCT01346319 |
| ABT-SLV361 | Other | Phase PHASE1 | Hypogonadal Males | COMPLETED | NCT01346319 |
| Standard Enteral Nutrition | Other | Phase PHASE3 | Respiratory Distress Syndrome,Adult | TERMINATED | NCT01464853 |
| Enteral nutrition with fatty acids | Other | Phase PHASE3 | Respiratory Distress Syndrome,Adult | TERMINATED | NCT01464853 |
| Standard Enteral Nutrition | Other | Phase PHASE3 | Respiratory Distress Syndrome,Adult | TERMINATED | NCT01464853 |
| Enteral nutrition with fatty acids | Other | Phase PHASE3 | Respiratory Distress Syndrome,Adult | TERMINATED | NCT01464853 |
| monofocal acrylic intraocular lens | Other | Phase PHASE3 | Cataract | COMPLETED | NCT00747227 |
| modified light transmission intraocular lens | Other | Phase PHASE3 | Cataract | COMPLETED | NCT00747227 |
| Adalimumab 40 mg subcutaneous (SC) every other week (EOW) | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00233571 |
| placebo | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT01114880 |
| adalimumab | Other | Phase PHASE3 | Ankylosing Spondylitis | COMPLETED | NCT01114880 |
| Glucerna SR | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00631774 |
| Glucerna SR | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00631774 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus-Infection | COMPLETED | NCT01153269 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus-Infection | COMPLETED | NCT01153269 |
| Lopinavir/Ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus-Infection | COMPLETED | NCT01153269 |
| Lung Function Analysis | Other | Preclinical | Respiratory Syncytial Viruses | COMPLETED | NCT00585481 |
| Samples collection for viral diagnosis | Other | Preclinical | Respiratory Syncytial Viruses | COMPLETED | NCT00585481 |
| Lung Function Analysis | Other | Preclinical | Respiratory Syncytial Viruses | COMPLETED | NCT00585481 |
| Samples collection for viral diagnosis | Other | Preclinical | Respiratory Syncytial Viruses | COMPLETED | NCT00585481 |
| SLV337 | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| Placebo | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| SLV337 | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| Placebo | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| SLV337 | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| Placebo | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT00924534 |
| PDL192 | Other | Phase PHASE1 | Cancer | COMPLETED | NCT00738764 |
| PDL192 | Other | Phase PHASE1 | Cancer | COMPLETED | NCT00738764 |
| TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent | Other | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00140101 |
| ZoMaxx™ Drug-Eluting Coronary Stent System | Drug | Phase PHASE2 | Coronary Disease | COMPLETED | NCT00140101 |
| Leuprolide acetate Depot Susp. 11.25 mg (Poland), 3.75 mg (Ukraine) | Other | Preclinical | Advanced Prostate Cancer | COMPLETED | NCT01078545 |
| Lopinavir/ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01076985 |
| Lopinavir/ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01076985 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Maxacalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Maxacalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Maxacalcitol | Other | Phase PHASE2 | Chronic Kidney Disease on Hemodialysis | COMPLETED | NCT00667576 |
| Paricalcitol | Other | Phase PHASE4 | Secondary Hyperparathyroidism | TERMINATED | NCT00664430 |
| Calcitriol | Other | Phase PHASE4 | Secondary Hyperparathyroidism | TERMINATED | NCT00664430 |
| Placebo Injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| paricalcitol injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| Placebo Injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| paricalcitol injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| Placebo Injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| paricalcitol injection 4 mcg/mL | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) Stage 5 | TERMINATED | NCT00616902 |
| atorvastatin calcium | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| simvastatin | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| rosuvastatin calcium | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| ABT-335 | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| atorvastatin calcium | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| simvastatin | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| rosuvastatin calcium | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| ABT-335 | Other | Phase PHASE3 | Mixed Dyslipidemia | COMPLETED | NCT00491530 |
| Placebo | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Zemplar (paricalcitol) capsules | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Zemplar (paricalcitol ) capsules | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Placebo | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Zemplar (paricalcitol) capsules | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Zemplar (paricalcitol ) capsules | Other | Phase PHASE2 | Diabetic Nephropathy | COMPLETED | NCT00421733 |
| Cytochrome P450 inhibitor | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| Blood Sample Collection | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| ABT-267 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| Cytochrome P450 inhibitor | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| Blood Sample Collection | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| ABT-267 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT01181427 |
| paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease | COMPLETED | NCT01071070 |
| paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease | COMPLETED | NCT01071070 |
| paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease | COMPLETED | NCT01071070 |
| Paricalcitol | Other | Phase PHASE4 | Cardiovascular Disease | COMPLETED | NCT01331317 |
| Nutritional Beverage | Other | Phase PHASE2 | Human Volunteers | COMPLETED | NCT01464385 |
| Nutritional Beverage | Other | Phase PHASE2 | Human Volunteers | COMPLETED | NCT01464385 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Disease | COMPLETED | NCT00631228 |
| Placebo Comparator | Other | Phase PHASE1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | COMPLETED | NCT01464320 |
| ABT-614 | Other | Phase PHASE1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | COMPLETED | NCT01464320 |
| Placebo Comparator | Other | Phase PHASE1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | COMPLETED | NCT01464320 |
| ABT-614 | Other | Phase PHASE1 | Type 2 Diabetics, Chronic Kidney Disease, Protein in Urine | COMPLETED | NCT01464320 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195650 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT00195650 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Tricuspid Transcatheter Edge-to-Edge Repair (TEER) | Other | Preclinical | Tricuspid Regurgitation (TR) | ENROLLING_BY_INVITATION | NCT07586995 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| lopinavir/ritonavir (LPV/r) (tablet or capsule) with nucleoside reverse transcriptase inhibitors (NRTIs) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infections | COMPLETED | NCT00262522 |
| lopinavir/ritonavir (LPV/r) (tablet or capsule) with nucleoside reverse transcriptase inhibitors (NRTIs) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infections | COMPLETED | NCT00262522 |
| Placebo | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00726440 |
| Navigator® | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00726440 |
| Placebo | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00726440 |
| Navigator® | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00726440 |
| raltegravir (RAL) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| lopinavir/ritonavir (LPV/r) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| raltegravir (RAL) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| lopinavir/ritonavir (LPV/r) | Other | Phase PHASE3 | Human Immunodeficiency Virus Infection | COMPLETED | NCT00711009 |
| placebo | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00109512 |
| NBI-56418 (GnRH antagonist) | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00109512 |
| placebo | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00109512 |
| NBI-56418 (GnRH antagonist) | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00109512 |
| Coronary angioplasty using the everolimus-eluting stent | Other | Phase PHASE4 | In-Stent Restenosis | UNKNOWN | NCT01239953 |
| Coronary angioplasty using the paclitaxel-eluting balloon | Other | Phase PHASE4 | In-Stent Restenosis | UNKNOWN | NCT01239953 |
| Lopinavir/ritonavir (Kaletra) | Other | Preclinical | Human Immunodeficiency Virus | COMPLETED | NCT01076972 |
| linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01381341 |
| Placebo | Other | Phase PHASE4 | Spondyloarthritis | UNKNOWN | NCT00477893 |
| Adalimumab | Other | Phase PHASE4 | Spondyloarthritis | UNKNOWN | NCT00477893 |
| Placebo | Other | Phase PHASE4 | Spondyloarthritis | UNKNOWN | NCT00477893 |
| Adalimumab | Other | Phase PHASE4 | Spondyloarthritis | UNKNOWN | NCT00477893 |
| Early discharge after percutaneous coronary intervenntion | Other | Preclinical | Coronary Artery Disease | TERMINATED | NCT00419055 |
| Early discharge after percutaneous coronary intervenntion | Other | Preclinical | Coronary Artery Disease | TERMINATED | NCT00419055 |
| placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT00420927 |
| XIENCE V® | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00987506 |
| Routine Care (RC) | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| 0SJ-IOMS | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| DAS28-IOMS | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| Routine Care (RC) | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| 0SJ-IOMS | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| DAS28-IOMS | Other | Preclinical | Rheumatoid Arthritis (RA) | COMPLETED | NCT01585064 |
| M200 (Volociximab), Carboplatin, Paclitaxel, Bevacizumab | Other | Phase PHASE1 | Non-small Cell Lung Cancer | COMPLETED | NCT00666692 |
| M200 (Volociximab), Carboplatin, Paclitaxel, Bevacizumab | Other | Phase PHASE1 | Non-small Cell Lung Cancer | COMPLETED | NCT00666692 |
| M200 (Volociximab), Carboplatin, Paclitaxel, Bevacizumab | Other | Phase PHASE1 | Non-small Cell Lung Cancer | COMPLETED | NCT00666692 |
| volociximab | Other | Phase PHASE2 | Stage IV Melanoma | TERMINATED | NCT00369395 |
| volociximab | Other | Phase PHASE2 | Stage IV Melanoma | TERMINATED | NCT00369395 |
| Visilizumab | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT00307827 |
| Visilizumab | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT00307827 |
| Volociximab (anti-α5β1 integrin monoclonal antibody) | Other | Phase PHASE2 | Renal Cell Carcinoma | TERMINATED | NCT00100685 |
| Volociximab (anti-α5β1 integrin monoclonal antibody) | Other | Phase PHASE2 | Renal Cell Carcinoma | TERMINATED | NCT00100685 |
| Volociximab (anti-α5β1 integrin monoclonal antibody) | Other | Phase PHASE2 | Renal Cell Carcinoma | TERMINATED | NCT00100685 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| ABT-126 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01482845 |
| Docetaxel | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| Docetaxel | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| Docetaxel | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00888108 |
| XIENCE PRIMETM everolimus-eluting coronary stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01605721 |
| Kaletra Tablets | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00508222 |
| Kaletra Tablets | Other | Phase PHASE3 | HIV Infections | COMPLETED | NCT00508222 |
| lopinavir /ritonavir plus two nucleosides | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT01237444 |
| lopinavir/ritonavir plus one nucleoside | Other | Phase PHASE3 | HIV Infection | COMPLETED | NCT01237444 |
| Soy formula experimental #2 | Other | Phase PHASE2 | Infant, Newborn | COMPLETED | NCT00798382 |
| Commercially available soy formula | Other | Phase PHASE2 | Infant, Newborn | COMPLETED | NCT00798382 |
| soy protein formula | Other | Phase PHASE2 | Infant, Newborn | COMPLETED | NCT00798382 |
| Cinacalcet | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00977080 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00977080 |
| Cinacalcet | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00977080 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00977080 |
| Xact Stent with either Emboshield Pro (Gen 5) or Emboshield (Gen 3) | Other | Approved | Carotid Artery Disease | COMPLETED | NCT00402740 |
| 6 Mercaptopurine | Other | Phase PHASE3 | Crohn Disease | UNKNOWN | NCT01629628 |
| Adalimumab | Other | Phase PHASE3 | Crohn Disease | UNKNOWN | NCT01629628 |
| 6 Mercaptopurine | Other | Phase PHASE3 | Crohn Disease | UNKNOWN | NCT01629628 |
| Adalimumab | Other | Phase PHASE3 | Crohn Disease | UNKNOWN | NCT01629628 |
| Propofol Target Controlled Infusion for Induction and Sevoflurane Inhalation for Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| Propofol Target Controlled Infusion for Induction and Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| Sevoflurane Inhalational Induction and Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| Propofol Target Controlled Infusion for Induction and Sevoflurane Inhalation for Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| Propofol Target Controlled Infusion for Induction and Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| Sevoflurane Inhalational Induction and Maintenance | Other | Phase PHASE4 | Elective Laparoscopic Surgery | COMPLETED | NCT01191476 |
| placebo | Other | Phase PHASE3 | Giant Cell Arteritis | COMPLETED | NCT00305539 |
| adalimumab | Other | Phase PHASE3 | Giant Cell Arteritis | COMPLETED | NCT00305539 |
| placebo | Other | Phase PHASE3 | Giant Cell Arteritis | COMPLETED | NCT00305539 |
| adalimumab | Other | Phase PHASE3 | Giant Cell Arteritis | COMPLETED | NCT00305539 |
| Dietary Counseling | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01641770 |
| Nutritional beverage 10003RF | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01641770 |
| Dietary Counseling | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01641770 |
| Nutritional beverage 10003RF | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01641770 |
| Placebo | Other | Phase PHASE3 | Hand Osteoarthritis | COMPLETED | NCT00597623 |
| Adalimumab (Humira®) | Other | Phase PHASE3 | Hand Osteoarthritis | COMPLETED | NCT00597623 |
| Placebo | Other | Phase PHASE3 | Hand Osteoarthritis | COMPLETED | NCT00597623 |
| Adalimumab (Humira®) | Other | Phase PHASE3 | Hand Osteoarthritis | COMPLETED | NCT00597623 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Prophylaxis of Influenza | COMPLETED | NCT01633749 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Prophylaxis of Influenza | COMPLETED | NCT01633749 |
| adalimumab (Humira) | Other | Preclinical | Psoriatic Arthritis | WITHDRAWN | NCT01078610 |
| adalimumab (Humira) | Other | Preclinical | Psoriatic Arthritis | WITHDRAWN | NCT01078610 |
| adalimumab (Humira) | Other | Preclinical | Psoriatic Arthritis | WITHDRAWN | NCT01078610 |
| Rifabutin | Other | Phase PHASE2 | HIV | UNKNOWN | NCT01663168 |
| Rifabutin | Other | Phase PHASE2 | HIV | UNKNOWN | NCT01663168 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Disease | COMPLETED | NCT00631228 |
| Intravenous anesthetic, propofol | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| Inhalational anesthetic | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| Intravenous anesthetic, propofol | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| Inhalational anesthetic | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| Intravenous anesthetic, propofol | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| Inhalational anesthetic | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00286585 |
| linifanib | Other | Phase PHASE1 | Advanced or Metastatic Solid Tumors | TERMINATED | NCT01506934 |
| linifanib | Other | Phase PHASE1 | Advanced or Metastatic Solid Tumors | TERMINATED | NCT01506934 |
| linifanib | Other | Phase PHASE1 | Advanced or Metastatic Solid Tumors | TERMINATED | NCT01506934 |
| Hospital food | Other | Phase PHASE3 | Burns | COMPLETED | NCT01464866 |
| Nutritional Supplement | Other | Phase PHASE3 | Burns | COMPLETED | NCT01464866 |
| Xience V® | Other | Phase PHASE3 | Coronary Restenosis | COMPLETED | NCT00882219 |
| Sorafenib | Other | Phase PHASE3 | Hepatocellular Carcinoma Non-resectable | TERMINATED | NCT01009593 |
| ABT-869 | Other | Phase PHASE3 | Hepatocellular Carcinoma Non-resectable | TERMINATED | NCT01009593 |
| Sorafenib | Other | Phase PHASE3 | Hepatocellular Carcinoma Non-resectable | TERMINATED | NCT01009593 |
| ABT-869 | Other | Phase PHASE3 | Hepatocellular Carcinoma Non-resectable | TERMINATED | NCT01009593 |
| FITC-Adalimumab | Other | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01275508 |
| FITC-Adalimumab | Other | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01275508 |
| SLV354 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT01545310 |
| ABT-869, linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | TERMINATED | NCT01286974 |
| [14C]linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | TERMINATED | NCT01286974 |
| ABT-869, linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | TERMINATED | NCT01286974 |
| [14C]linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | TERMINATED | NCT01286974 |
| Experimental Study Formula | Other | Phase PHASE3 | Healthy Infants | COMPLETED | NCT01699386 |
| Control Study Formula | Other | Phase PHASE3 | Healthy Infants | COMPLETED | NCT01699386 |
| Synagis (palivizumab), monoclonal antibody for passive immunoprophylaxis against severe RSV disease administered according to usual clinical practice. | Other | Preclinical | Respiratory Syncytial Virus Infection | COMPLETED | NCT01107535 |
| Synagis (palivizumab), monoclonal antibody for passive immunoprophylaxis against severe RSV disease administered according to usual clinical practice. | Other | Preclinical | Respiratory Syncytial Virus Infection | COMPLETED | NCT01107535 |
| Synagis (palivizumab), monoclonal antibody for passive immunoprophylaxis against severe RSV disease administered according to usual clinical practice. | Other | Preclinical | Respiratory Syncytial Virus Infection | COMPLETED | NCT01107535 |
| leuprolide (Lucrin/Lucrin-Tri-depot) | Other | Preclinical | Prostatic Neoplasm | COMPLETED | NCT01081873 |
| leuprolide (Lucrin/Lucrin-Tri-depot) | Other | Preclinical | Prostatic Neoplasm | COMPLETED | NCT01081873 |
| leuprolide (Lucrin/Lucrin-Tri-depot) | Other | Preclinical | Prostatic Neoplasm | COMPLETED | NCT01081873 |
| Clinical evaluations/Blood draws | Other | Approved | HIV Infections | COMPLETED | NCT00571961 |
| buprenorphine | Other | Approved | HIV Infections | COMPLETED | NCT00571961 |
| Kaletra (lopinavir/ritonavir) | Other | Approved | HIV Infections | COMPLETED | NCT00571961 |
| A powdered milk-based infant formula, standard fat blend | Other | Phase PHASE3 | Healthy Term Infant | COMPLETED | NCT01617889 |
| Experimental powdered milk-based infant formula with an alternate fat blend | Other | Phase PHASE3 | Healthy Term Infant | COMPLETED | NCT01617889 |
| Experimental Hydrolyzed infant formula | Other | Phase PHASE3 | Infant | COMPLETED | NCT01573871 |
| Experimental Hydrolyzed infant formula | Other | Phase PHASE3 | Infant | COMPLETED | NCT01573871 |
| Experimental Infant Formula | Other | Approved | Growth and Tolerance Infant Study | COMPLETED | NCT01812629 |
| Lopinavir/ritonavir (drug) | Drug | Phase PHASE3 | HIV Infections | COMPLETED | NCT00140751 |
| Lopinavir/ritonavir (drug) | Drug | Phase PHASE3 | HIV Infections | COMPLETED | NCT00140751 |
| divalproex sodium extended release | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00181727 |
| Low dose Kaletra tablets | Other | Approved | HIV Infections | COMPLETED | NCT00762320 |
| Low dose Kaletra tablets | Other | Approved | HIV Infections | COMPLETED | NCT00762320 |
| Low dose Kaletra tablets | Other | Approved | HIV Infections | COMPLETED | NCT00762320 |
| Placebo | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| Placebo | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| Placebo | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| Paricalcitol | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01003275 |
| No treatment | Drug | Preclinical | Type 1 Diabetes | COMPLETED | NCT02073058 |
| No treatment | Drug | Preclinical | Type 1 Diabetes | COMPLETED | NCT02073058 |
| Amino Acid Supplement Group | Other | Preclinical | Wounds | COMPLETED | NCT02146612 |
| Amino Acid Supplement Group | Other | Preclinical | Wounds | COMPLETED | NCT02146612 |
| CCC Surgery | Procedure | Phase PHASE3 | Cataract | COMPLETED | NCT01069172 |
| FS Laser Surgery | Procedure | Phase PHASE3 | Cataract | COMPLETED | NCT01069172 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| TAXUS™ EXPRESS2™ Paclitaxel Eluting Coronary Stent | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00307047 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00307047 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00676520 |
| XIENCE V® Everolimus Eluting Coronary Stent | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00676520 |
| Temozolomide | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| veliparib | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| Temozolomide | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| veliparib | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| Temozolomide | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| veliparib | Other | Phase PHASE2 | Solid Tumor Cancers | COMPLETED | NCT01193140 |
| Adalimumab | Other | Phase PHASE2 | Uveitis | UNKNOWN | NCT00348153 |
| Adalimumab | Other | Phase PHASE2 | Uveitis | UNKNOWN | NCT00348153 |
| protein and meal frequency | Other | Approved | Obesity | COMPLETED | NCT01749449 |
| protein and meal frequency | Other | Approved | Obesity | COMPLETED | NCT01749449 |
| Herculink Elite Renal Stent System | Other | Approved | Renal Artery Obstruction | COMPLETED | NCT00490841 |
| Coronary artery placement of a drug-eluting stent | Drug | Preclinical | Coronary Disease | COMPLETED | NCT01310309 |
| Buffered pantoprazole | Other | Phase PHASE4 | Acid Peptic Disorder | COMPLETED | NCT01214408 |
| Buffered pantoprazole | Other | Phase PHASE4 | Acid Peptic Disorder | COMPLETED | NCT01214408 |
| Buffered pantoprazole | Other | Phase PHASE4 | Acid Peptic Disorder | COMPLETED | NCT01214408 |
| Rhythm control | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00578617 |
| Rhythm Control | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00578617 |
| Rate control | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00578617 |
| Ablation Therapy | Drug | Approved | Atrial Fibrillation | COMPLETED | NCT00578617 |
| Rate Control | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00578617 |
| Experimental oral medical nutritional supplement with AN777 | Other | Phase PHASE3 | Elderly | COMPLETED | NCT01483976 |
| Oral medical nutritional supplement | Other | Phase PHASE3 | Elderly | COMPLETED | NCT01483976 |
| Experimental oral medical nutritional supplement with AN777 | Other | Phase PHASE3 | Elderly | COMPLETED | NCT01483976 |
| Oral medical nutritional supplement | Other | Phase PHASE3 | Elderly | COMPLETED | NCT01483976 |
| Study Oral Nutritional Supplement | Other | Approved | Gastro-intestinal Tolerance | COMPLETED | NCT01781624 |
| Clarithromycin modified release 500 mg | Other | Preclinical | Bronchitis | COMPLETED | NCT01354938 |
| clarithromycin modified release 500 mg | Other | Preclinical | Respiratory Tract Infection | COMPLETED | NCT01075204 |
| clarithromycin modified release 500 mg | Other | Preclinical | Respiratory Tract Infection | COMPLETED | NCT01075204 |
| Placebo | Other | Approved | Type 2 Diabetes | UNKNOWN | NCT01792206 |
| Zemplar | Other | Approved | Type 2 Diabetes | UNKNOWN | NCT01792206 |
| A powdered milk-based infant formula, standard fat blend | Other | Phase PHASE3 | Healthy Term Infant | COMPLETED | NCT01617889 |
| Experimental powdered milk-based infant formula with an alternate fat blend | Other | Phase PHASE3 | Healthy Term Infant | COMPLETED | NCT01617889 |
| Experimental Oral Nutritional Supplement | Other | Phase PHASE3 | Pneumonia | TERMINATED | NCT01477723 |
| Experimental Oral Nutritional Supplement | Other | Phase PHASE3 | Pneumonia | TERMINATED | NCT01477723 |
| Infant formula powder | Other | Phase PHASE3 | Infant Newborn | COMPLETED | NCT01380886 |
| experimental infant formula with alternate protein source | Other | Phase PHASE3 | Infant Newborn | COMPLETED | NCT01380886 |
| Infant formula powder | Other | Phase PHASE3 | Infant Newborn | COMPLETED | NCT01380886 |
| experimental infant formula with alternate protein source | Other | Phase PHASE3 | Infant Newborn | COMPLETED | NCT01380886 |
| Control human milk fortifier | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT01373073 |
| Experimental human milk fortifier | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT01373073 |
| Control human milk fortifier | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT01373073 |
| Experimental human milk fortifier | Other | Phase PHASE3 | Preterm Infants | COMPLETED | NCT01373073 |
| oral nutritional formula | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01191125 |
| medical food with AN777 | Other | Phase PHASE3 | Malnutrition | COMPLETED | NCT01191125 |
| Experimental Infant Formula | Other | Approved | Protein Sensitive Colitis | COMPLETED | NCT01813526 |
| Experimental Infant Formula | Other | Approved | Protein Sensitive Colitis | COMPLETED | NCT01813526 |
| Monotherapy (Lopinavir/ritonavir) + ABC/3TC | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Monotherapy (Lopinavir/ritonavir) | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Monotherapy (Lopinavir/ritonavir) + ABC/3TC | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Monotherapy (Lopinavir/ritonavir) | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Monotherapy (Lopinavir/ritonavir) + ABC/3TC | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Monotherapy (Lopinavir/ritonavir) | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865007 |
| Experimental Infant Formula | Other | Approved | Growth and Tolerance Infant Study | COMPLETED | NCT01820494 |
| Radiofrequency catheter ablation | Other | Phase PHASE4 | Supraventricular Tachycardias | COMPLETED | NCT01132274 |
| iFS™ Femtosecond Laser System | Other | Approved | Refractive Astigmatism | COMPLETED | NCT01210820 |
| Corticosteroid Avoidance Immune Suppression Protocol | Other | Approved | Transplant; Failure, Kidney | COMPLETED | NCT00587158 |
| Paricalcitol | Other | Approved | Transplant; Failure, Kidney | COMPLETED | NCT00587158 |
| Corticosteroid Avoidance Immune Suppression Protocol | Other | Approved | Transplant; Failure, Kidney | COMPLETED | NCT00587158 |
| Paricalcitol | Other | Approved | Transplant; Failure, Kidney | COMPLETED | NCT00587158 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT01163162 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT01163162 |
| adalimumab | Other | Phase PHASE2 | Sarcoidosis | COMPLETED | NCT00274352 |
| adalimumab | Other | Phase PHASE2 | Sarcoidosis | COMPLETED | NCT00274352 |
| OptiFree PureMoist | Other | Approved | Contact Lens Solution Toxicity | UNKNOWN | NCT01847105 |
| RevitaLens | Other | Approved | Contact Lens Solution Toxicity | UNKNOWN | NCT01847105 |
| Placebo (soybean oil and dl-alpha-tocopheryl acetate) | Other | Phase PHASE3 | Lactation | COMPLETED | NCT01747668 |
| Similac Prenatal Vitamin soft-gel capsule | Other | Phase PHASE3 | Lactation | COMPLETED | NCT01747668 |
| Study Oral Nutritional Supplement | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT01782456 |
| Placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Itopride HCI 100 mg | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Itopride HCI 50 mg | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Itopride HCI 100 mg | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Itopride HCI 50 mg | Other | Phase PHASE2 | Irritable Bowel Syndrome | COMPLETED | NCT01027260 |
| Eicosapentaenoic acid enriched nutritional supplement | Other | Phase PHASE4 | Colorectal Neoplasms | TERMINATED | NCT00398333 |
| Eicosapentaenoic acid enriched nutritional supplement | Other | Phase PHASE4 | Colorectal Neoplasms | TERMINATED | NCT00398333 |
| Eicosapentaenoic acid enriched nutritional supplement | Other | Phase PHASE4 | Colorectal Neoplasms | TERMINATED | NCT00398333 |
| Abound (7 g of Arginine, 7 g Glutamine and 1.2 g HMB) | Other | Approved | Pressure Ulcer | COMPLETED | NCT01090076 |
| Abound (7 g of Arginine, 7 g Glutamine and 1.2 g HMB) | Other | Approved | Pressure Ulcer | COMPLETED | NCT01090076 |
| Study product containing lutein | Other | Phase PHASE3 | Healthy Subjects | COMPLETED | NCT01730898 |
| Triage® B-Type Natriuretic Peptide (BNP) Test | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00206856 |
| Zemplar | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01204528 |
| Zemplar | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01204528 |
| Zemplar | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01204528 |
| Switching to LPV/r monotherapy (Kaletra) | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865475 |
| AZT+3TC+ABV (Trizivir) | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865475 |
| Switching to LPV/r monotherapy (Kaletra) | Drug | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865475 |
| AZT+3TC+ABV (Trizivir) | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00865475 |
| divalproex sodium extended release | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00181727 |
| Placebo | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| Cell-Derived Trivalent Subunit Influenza Vaccine | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| Placebo | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| Cell-Derived Trivalent Subunit Influenza Vaccine | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| Placebo | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| Cell-Derived Trivalent Subunit Influenza Vaccine | Other | Phase PHASE2 | Influenza | COMPLETED | NCT00889889 |
| STAR S4IR LASIK with VSS-R ablation profile | Other | Approved | Refractive Error | COMPLETED | NCT01067716 |
| divalproex | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| olanzapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| quetiapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| risperidone | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| divalproex | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| olanzapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| quetiapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| risperidone | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| divalproex | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| olanzapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| quetiapine | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| risperidone | Other | Phase PHASE4 | Senile Dementia, Alzheimer Type | COMPLETED | NCT00208819 |
| Levosimendan | Other | Phase PHASE3 | Heart Failure | TERMINATED | NCT00166127 |
| Levosimendan | Other | Phase PHASE3 | Heart Failure | TERMINATED | NCT00166127 |
| receive amino acid supplement | Other | Approved | Obesity | COMPLETED | NCT00473356 |
| receive amino acid supplement | Other | Approved | Obesity | COMPLETED | NCT00473356 |
| LPV/r | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00148759 |
| LPV/r | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00148759 |
| carotenoids | Other | Approved | Retinopathy of Prematurity | COMPLETED | NCT00872664 |
| carotenoids | Other | Approved | Retinopathy of Prematurity | COMPLETED | NCT00872664 |
| carotenoids | Other | Approved | Retinopathy of Prematurity | COMPLETED | NCT00872664 |
| Opti-Free | Other | Phase PHASE3 | Study Focus is Healthy Contact Lens Wearers | COMPLETED | NCT00961051 |
| Investigational MPS | Other | Phase PHASE3 | Study Focus is Healthy Contact Lens Wearers | COMPLETED | NCT00961051 |
| Without selenium and sodium selenite supplementation | Other | Approved | Preterm Infants | COMPLETED | NCT02066610 |
| Without selenium and sodium selenate supplementation | Other | Approved | Preterm Infants | COMPLETED | NCT02066610 |
| selenium and sodium selenite supplementation | Other | Approved | Preterm Infants | COMPLETED | NCT02066610 |
| selenium and sodium selenate supplementation | Other | Approved | Preterm Infants | COMPLETED | NCT02066610 |
| crystalens Accommodating IOL | Other | Phase PHASE4 | Cataract | COMPLETED | NCT01275118 |
| Tecnis Multifocal IOL | Other | Phase PHASE4 | Cataract | COMPLETED | NCT01275118 |
| Ensure powder | Other | Approved | Malnourished | COMPLETED | NCT01421680 |
| Ensure powder | Other | Approved | Malnourished | COMPLETED | NCT01421680 |
| Treatment Algorithm for Crohn's Disease | Drug | Phase PHASE4 | Crohn's Disease | COMPLETED | NCT01030809 |
| Testosterone | Other | Phase PHASE1 | Obesity | COMPLETED | NCT01160328 |
| Leuprolide | Other | Phase PHASE1 | Obesity | COMPLETED | NCT01160328 |
| placebo | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| paricalcitol | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| placebo | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| paricalcitol | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| placebo | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| paricalcitol | Other | Phase PHASE3 | Coronary Artery Disease | TERMINATED | NCT01012414 |
| iFS Femtosecond Laser System | Other | Phase PHASE2 | Corneal Astigmatism | COMPLETED | NCT01348854 |
| iFS Femtosecond Laser System | Other | Phase PHASE2 | Corneal Astigmatism | COMPLETED | NCT01348854 |
| Niacin | Other | Preclinical | Cardiovascular Diseases | COMPLETED | NCT01200160 |
| Niacin | Other | Preclinical | Cardiovascular Diseases | COMPLETED | NCT01200160 |
| Meals on Wheels | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Ensure Plus | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Meals on Wheels | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Ensure Plus | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Meals on Wheels | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Ensure Plus | Other | Approved | Elderly | COMPLETED | NCT00933153 |
| Creon 25000 matching Placebo | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | WITHDRAWN | NCT02009410 |
| Creon | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | WITHDRAWN | NCT02009410 |
| Creon 25000 matching Placebo | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | WITHDRAWN | NCT02009410 |
| Creon | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency in Subjects With Diabetes Mellitus Type 2 | WITHDRAWN | NCT02009410 |
| lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00946595 |
| efavirenz/emtricitabin/tenofovir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00946595 |
| lopinavir/ritonavir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00946595 |
| efavirenz/emtricitabin/tenofovir | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00946595 |
| Pancreatin | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency | COMPLETED | NCT01747330 |
| Pancreatin | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency | COMPLETED | NCT01747330 |
| Implanted device and lead (Cardiac Resynchronization Therapy Defibrillator (CRT-D) device and SJM Quadripolar lead system) | Drug | Phase PHASE4 | Heart Failure | UNKNOWN | NCT02195843 |
| Anatomical optimization of device and leads | Device | Phase PHASE4 | Heart Failure | UNKNOWN | NCT02195843 |
| Electrical optimization by RVLV Conduction Time with VectSelect | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT02195843 |
| Placebo Eprosartan | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Placebo Eprosartan mesylate | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Eprosartan Mesylate | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Eprosartan | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Placebo Eprosartan | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Placebo Eprosartan mesylate | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Eprosartan Mesylate | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Eprosartan | Other | Phase PHASE3 | Essential Hypertension | COMPLETED | NCT01631227 |
| Jevity 1.5 | Other | Approved | Acute Lung Injury | UNKNOWN | NCT02208700 |
| Oxepa | Other | Approved | Acute Lung Injury | UNKNOWN | NCT02208700 |
| Everolimus eluting stents | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01776567 |
| ABT-510 | Other | Phase PHASE1 | Head and Neck Cancer | COMPLETED | NCT00113334 |
| ABT-510 | Other | Phase PHASE1 | Head and Neck Cancer | COMPLETED | NCT00113334 |
| Percutaneous Coronary Intervention using bare metal stents | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02198716 |
| Percutaneous Coronary Intervention using drug eluting stents | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT02198716 |
| 4 mm punch biopsies | Other | Preclinical | Psoriasis | UNKNOWN | NCT01604902 |
| 4 mm punch biopsies | Other | Preclinical | Psoriasis | UNKNOWN | NCT01604902 |
| 4 mm punch biopsies | Other | Preclinical | Psoriasis | UNKNOWN | NCT01604902 |
| lopinavir/ritonavir; nevirapine; Zidovudine; Lamivudine | Other | Phase PHASE4 | HIV | COMPLETED | NCT00143689 |
| Valproate | Other | Phase PHASE4 | Schizophrenia | COMPLETED | NCT00194025 |
| Valproate | Other | Phase PHASE4 | Schizophrenia | COMPLETED | NCT00194025 |
| fenofibrate | Other | Phase PHASE4 | Dyslipidemias | COMPLETED | NCT01462877 |
| fenofibrate | Other | Phase PHASE4 | Dyslipidemias | COMPLETED | NCT01462877 |
| Ultrasonography | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01205854 |
| Ultrasonography | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01205854 |
| Emboshield NAV6® embolic protection system (Abbott Vascular, Santa Clara, CA) | Other | Approved | Carotid Artery Stenosis | UNKNOWN | NCT01550835 |
| Quetiapine | Other | Phase PHASE4 | Alzheimer's Disease | WITHDRAWN | NCT00375557 |
| Divalproex ER | Other | Phase PHASE4 | Alzheimer's Disease | WITHDRAWN | NCT00375557 |
| Counseling | Other | Approved | Children | TERMINATED | NCT02125123 |
| Nutritional Supplement and Counseling | Other | Approved | Children | TERMINATED | NCT02125123 |
| placebo | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT02245360 |
| Phleum pratense grass pollen allergen extract | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT02245360 |
| placebo | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT02245360 |
| Phleum pratense grass pollen allergen extract | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT02245360 |
| pediatric formula | Other | Preclinical | GI Tolerance | COMPLETED | NCT02819401 |
| Veliparib | Other | Phase PHASE1 | Recurrent, Epithelial Ovarian Cancer | COMPLETED | NCT01472783 |
| Veliparib | Other | Phase PHASE1 | Recurrent, Epithelial Ovarian Cancer | COMPLETED | NCT01472783 |
| Veliparib | Other | Phase PHASE1 | Recurrent, Epithelial Ovarian Cancer | COMPLETED | NCT01472783 |
| Nutritional Education | Other | Phase PHASE4 | Malnutrition | WITHDRAWN | NCT02360722 |
| Oral Nutritional Supplement | Other | Phase PHASE4 | Malnutrition | WITHDRAWN | NCT02360722 |
| Health Log | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT01913080 |
| Health Log | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT01913080 |
| Health Log | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT01913080 |
| Libra Deep Brain Stimulation System | Other | Approved | Treatment Resistant Depression | UNKNOWN | NCT01801319 |
| Libra Deep Brain Stimulation System | Other | Approved | Treatment Resistant Depression | UNKNOWN | NCT01801319 |
| Fractional flow reserve | Other | Phase PHASE4 | NonST Elevation Myocardial Infarction | UNKNOWN | NCT01764334 |
| Fractional flow reserve | Other | Phase PHASE4 | NonST Elevation Myocardial Infarction | UNKNOWN | NCT01764334 |
| placebo | Other | Phase PHASE4 | Gait or Balance Disorder Problems | COMPLETED | NCT01468285 |
| betahistine dihydrochloride | Other | Phase PHASE4 | Gait or Balance Disorder Problems | COMPLETED | NCT01468285 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Approved | Diabetes Mellitus | COMPLETED | NCT02665455 |
| CHO Experimental 4 Maltodextrin | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03293706 |
| CHO Experimental 3 Low Sugar | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03293706 |
| CHO Experimental 2 Digestion Resistant | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03293706 |
| CHO Experimental 1 Slowly Digested | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03293706 |
| CHO Control 1 and 2 Glucose | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03293706 |
| Nerve Block with Sham Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Nerve Block with Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Nerve Block with Sham Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Nerve Block with Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Nerve Block with Sham Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Nerve Block with Radiofrequency Ablation | Other | Approved | Chronic Knee Pain | COMPLETED | NCT02931435 |
| Device settings for group B | Device | Approved | Cardiac Death | COMPLETED | NCT01217528 |
| device settings for group A | Device | Approved | Cardiac Death | COMPLETED | NCT01217528 |
| Accent Pacemaker | Other | Approved | Sick Sinus Syndrome | TERMINATED | NCT01074749 |
| Quadripolar LV lead (pacing configurations) | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00964938 |
| Quadripolar LV lead (pacing configurations) | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00964938 |
| ICD Implantation | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT00949000 |
| SJ4 connector and RV high voltage SJ4 lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00940888 |
| SJ4 connector and RV high voltage SJ4 lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00940888 |
| ICD Implantation | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00919373 |
| VT ablation | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00919373 |
| Substrate modification | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00919373 |
| Pacing interventions | Other | Preclinical | Premature Ventricular Complexes | TERMINATED | NCT00888667 |
| ICD/ CRT-D | Other | Preclinical | Sudden Cardiac Death | COMPLETED | NCT00874445 |
| ICD | Other | Preclinical | Healthy | COMPLETED | NCT00873691 |
| Tendril Lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00870324 |
| OptiSense Lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00870324 |
| Tendril Lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00870324 |
| OptiSense Lead | Other | Preclinical | Tachyarrhythmias | COMPLETED | NCT00870324 |
| CRM Device | Device | Preclinical | Atrial Fibrillation | COMPLETED | NCT00837798 |
| VentricularAutoCaptureTM & ACapTM Confirm | Other | Preclinical | Pacemaker | COMPLETED | NCT00832988 |
| Cardiac Resynchronization Therapy implant | Drug | Approved | Heart Failure | COMPLETED | NCT00819117 |
| CRT-D (Intra-thoracic Impedance Monitoring) | Other | Preclinical | Heart Failure | COMPLETED | NCT00811551 |
| CRT-D (Intra-thoracic Impedance Monitoring) | Other | Preclinical | Heart Failure | COMPLETED | NCT00811551 |
| CRT-D (Intra-thoracic Impedance Monitoring) | Other | Preclinical | Heart Failure | COMPLETED | NCT00811551 |
| 3D echo-guided LV lead placement | Other | Approved | Heart Failure | COMPLETED | NCT01278030 |
| Therapy Cool Path Duo | Drug | Phase PHASE3 | Typical Atrial Flutter | COMPLETED | NCT00984204 |
| PVI + Defragmentation + linear lesions | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01580124 |
| PVI alone | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01580124 |
| Freestyle LIbre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03820050 |
| Folic Acid | Other | Phase PHASE2 | Oligoarthritis | COMPLETED | NCT04154852 |
| Placebo | Other | Phase PHASE2 | Oligoarthritis | COMPLETED | NCT04154852 |
| Methotrexate | Other | Phase PHASE2 | Oligoarthritis | COMPLETED | NCT04154852 |
| Adalimumab | Other | Phase PHASE2 | Oligoarthritis | COMPLETED | NCT04154852 |
| lopinavir/ritonavir plus maraviroc | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT01068873 |
| lopinavir/ritonavir plus maraviroc | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT01068873 |
| General Anesthetics | Other | Phase PHASE4 | Renal Injury | TERMINATED | NCT03940651 |
| Spinal Anesthesia | Other | Phase PHASE4 | Renal Injury | TERMINATED | NCT03940651 |
| blood taking | Other | Preclinical | Chest Pain | COMPLETED | NCT02789904 |
| HeartMate 3™ | Other | Approved | Heart Failure | COMPLETED | NCT02475460 |
| Less Invasive Surgery (LIS) | Procedure | Approved | Heart Failure | COMPLETED | NCT02475460 |
| Tricholoracetic acid | Other | Approved | Warts | COMPLETED | NCT05712811 |
| CRYOTHERAPY | Drug | Approved | Warts | COMPLETED | NCT05712811 |
| Electrophysiological study and bi-atrial Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study and Right side Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| i-STAT TBI Test | Other | Approved | Traumatic Brain Injury | RECRUITING | NCT06766435 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Partially Hydrolyzed Infant Formula | Other | Approved | Feeding Intolerance | TERMINATED | NCT02028156 |
| fenoldopam | Other | Phase PHASE2 | Kidney Failure, Acute | COMPLETED | NCT00122018 |
| N-acetylcysteine | Other | Phase PHASE2 | Kidney Failure, Acute | COMPLETED | NCT00122018 |
| fenoldopam | Other | Phase PHASE2 | Kidney Failure, Acute | COMPLETED | NCT00122018 |
| N-acetylcysteine | Other | Phase PHASE2 | Kidney Failure, Acute | COMPLETED | NCT00122018 |
| ABSORB implantation | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT02004730 |
| paricalcitol | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| gemcitabine hydrochloride | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| paricalcitol | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| gemcitabine hydrochloride | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| paricalcitol | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| gemcitabine hydrochloride | Other | Phase PHASE1 | Unspecified Adult Solid Tumor, Protocol Specific | COMPLETED | NCT00217477 |
| Simvastatin 40 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fixed Combination of Fenofibrate/simvastatin 145/40 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fenofibrate 145 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Simvastatin 20 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fixed Combination of Fenofibrate/simvastatin 145/20 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Simvastatin 40 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fixed Combination of Fenofibrate/simvastatin 145/40 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fenofibrate 145 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Simvastatin 20 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Fixed Combination of Fenofibrate/simvastatin 145/20 mg | Other | Phase PHASE3 | Dyslipidemia | COMPLETED | NCT01674712 |
| Pre-study antiretroviral regimen | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00700115 |
| Kaletra + Isentress | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00700115 |
| Pre-study antiretroviral regimen | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00700115 |
| Kaletra + Isentress | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00700115 |
| Clarithromycin | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002336 |
| Clofazimine | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Clarithromycin | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Ethambutol hydrochloride | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Clofazimine | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Clarithromycin | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Ethambutol hydrochloride | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Clofazimine | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Clarithromycin | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| Ethambutol hydrochloride | Other | Approved | Mycobacterium Avium-intracellular Infection | COMPLETED | NCT00002331 |
| nutritional supplement | Other | Phase PHASE3 | Children | COMPLETED | NCT01658267 |
| NGAL kit | Other | Preclinical | Heart Failure | COMPLETED | NCT00874289 |
| NGAL kit | Other | Preclinical | Heart Failure | COMPLETED | NCT00874289 |
| Placebo | Other | Phase PHASE3 | Hypogonadism | COMPLETED | NCT00433199 |
| Testosterone (T) Gel 1.62% | Other | Phase PHASE3 | Hypogonadism | COMPLETED | NCT00433199 |
| Placebo | Other | Phase PHASE3 | Hypogonadism | COMPLETED | NCT00433199 |
| Testosterone (T) Gel 1.62% | Other | Phase PHASE3 | Hypogonadism | COMPLETED | NCT00433199 |
| Humira Then Humira plus 3 B vitamins | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT01704599 |
| Humira Then Humira plus 3 B vitamins | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT01704599 |
| Oral Nutritional Supplement | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT01902212 |
| Control Study Product | Other | Approved | Diabetes | COMPLETED | NCT01850810 |
| Experimental Study Product | Other | Approved | Diabetes | COMPLETED | NCT01850810 |
| Control Study Product | Other | Approved | Diabetes | COMPLETED | NCT01850810 |
| Experimental Study Product | Other | Approved | Diabetes | COMPLETED | NCT01850810 |
| Peptide based enteral formula | Other | Phase PHASE3 | Gastrointestinal Diseases | COMPLETED | NCT01191112 |
| Placebo | Other | Phase PHASE4 | Flushing | COMPLETED | NCT00913081 |
| Quercetin | Other | Phase PHASE4 | Flushing | COMPLETED | NCT00913081 |
| Placebo | Other | Phase PHASE4 | Flushing | COMPLETED | NCT00913081 |
| Quercetin | Other | Phase PHASE4 | Flushing | COMPLETED | NCT00913081 |
| Dietary Counseling | Other | Approved | Growth | COMPLETED | NCT02056275 |
| Nutrition supplement + dietary counseling | Other | Approved | Growth | COMPLETED | NCT02056275 |
| Dietary Counseling | Other | Approved | Growth | COMPLETED | NCT02056275 |
| Nutrition supplement + dietary counseling | Other | Approved | Growth | COMPLETED | NCT02056275 |
| Monofocal Intraocular Lens | Other | Phase PHASE1 | Cataract | COMPLETED | NCT01714635 |
| Tecnis Multifocal Intraocular Lens | Other | Phase PHASE1 | Cataract | COMPLETED | NCT01714635 |
| Monofocal Intraocular Lens | Other | Phase PHASE1 | Cataract | COMPLETED | NCT01714635 |
| Tecnis Multifocal Intraocular Lens | Other | Phase PHASE1 | Cataract | COMPLETED | NCT01714635 |
| Investigational Milk-based Formula Containing Carotenoid | Other | Approved | Infants | TERMINATED | NCT02069522 |
| Standard Milk-based Formula Containing Carotenoid | Other | Approved | Infants | TERMINATED | NCT02069522 |
| Lopinavir/r plus saquinavir | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00476359 |
| Lopinavir/r plus saquinavir | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00476359 |
| Nutritional Supplement | Other | Preclinical | Malnutrition | UNKNOWN | NCT02404987 |
| Percutaneous coronary intervention (PCI) | Other | Phase PHASE4 | Coronary Occlusion | COMPLETED | NCT00987610 |
| XIENCE V®/ XIENCE PRIME™ | Other | Phase PHASE4 | Coronary Artery Stenosis | COMPLETED | NCT00496938 |
| Multi-Link Frontier Coronary Stent System | Other | Phase PHASE4 | Coronary Artery Disease | WITHDRAWN | NCT00286195 |
| Placebo | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT02187757 |
| Study Dietary Supplement (Prelipid 500 mg capsules) | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT02187757 |
| Placebo | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT02187757 |
| Study Dietary Supplement (Prelipid 500 mg capsules) | Other | Phase PHASE3 | Hyperlipidemia | COMPLETED | NCT02187757 |
| Lopinavir | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00771498 |
| Lopinavir | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00771498 |
| Quetiapine | Other | Phase PHASE4 | Alzheimer's Disease | WITHDRAWN | NCT00375557 |
| Divalproex ER | Other | Phase PHASE4 | Alzheimer's Disease | WITHDRAWN | NCT00375557 |
| Active Comparator: Control Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 3 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 2 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 1 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Active Comparator: Control Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 3 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 2 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Experimental Infant Formula 1 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02456831 |
| Xience Prime Long Lesion (LL) | Other | Phase PHASE3 | Myocardial Ischemia | COMPLETED | NCT00916370 |
| Core size Xience Prime | Other | Phase PHASE3 | Myocardial Ischemia | COMPLETED | NCT00916370 |
| Absolute Pro™ Peripheral Self-Expanding Stent System | Other | Phase PHASE3 | Peripheral Vascular Disease | COMPLETED | NCT00844532 |
| Absolute Pro™ Peripheral Self-Expanding Stent System | Other | Phase PHASE3 | Peripheral Vascular Disease | COMPLETED | NCT00844532 |
| Topotecan | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT01690598 |
| Veliparib | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT01690598 |
| Ademetionine tablet | Other | Phase PHASE3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | COMPLETED | NCT02200029 |
| Ademetionine IV+tablet | Other | Phase PHASE3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | COMPLETED | NCT02200029 |
| Ademetionine tablet | Other | Phase PHASE3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | COMPLETED | NCT02200029 |
| Ademetionine IV+tablet | Other | Phase PHASE3 | Intrahepatic Cholestasis Associated With Alcoholic Liver Disease | COMPLETED | NCT02200029 |
| XIENCE V® EECSS | Other | Preclinical | Chronic Coronary Occlusion | COMPLETED | NCT01120379 |
| Osmolite 1.2 | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| VITAL AF | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| Osmolite 1.2 | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| VITAL AF | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| Osmolite 1.2 | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| VITAL AF | Other | Approved | Critical Illness | COMPLETED | NCT01448135 |
| lopinavir/ritonavir plus maraviroc | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT00981318 |
| Lopinavir/Ritonavir (200/50 mg) Tablets + Zidovudine + 3TC | Other | Phase PHASE4 | HIV | COMPLETED | NCT01088516 |
| Lopinavir/Ritonavir (200/50 mg) Tablets + Zidovudine + 3TC | Other | Phase PHASE4 | HIV | COMPLETED | NCT01088516 |
| Ritonavir-boosted lopinavir | Other | Phase PHASE4 | HIV-1 | COMPLETED | NCT01192035 |
| Efavirenz or Nevirapine | Other | Phase PHASE4 | HIV-1 | COMPLETED | NCT01192035 |
| Ritonavir-boosted lopinavir | Other | Phase PHASE4 | HIV-1 | COMPLETED | NCT01192035 |
| Efavirenz or Nevirapine | Other | Phase PHASE4 | HIV-1 | COMPLETED | NCT01192035 |
| Bioabsorbable everolimus-eluting stent deployment | Other | Phase PHASE2 | Impotence, Arteriogenic | UNKNOWN | NCT02492386 |
| Bioabsorbable everolimus-eluting stent deployment | Other | Phase PHASE2 | Impotence, Arteriogenic | UNKNOWN | NCT02492386 |
| Nutritional management protocol | Other | Phase PHASE4 | Critical Illness | COMPLETED | NCT00574431 |
| Data Collection | Other | Phase PHASE4 | Critical Illness | COMPLETED | NCT00574431 |
| inactive drug | Drug | Phase PHASE3 | Interstitial Cystitis | COMPLETED | NCT01295814 |
| Adalimumab | Other | Phase PHASE3 | Interstitial Cystitis | COMPLETED | NCT01295814 |
| Fluvoxamine | Other | Phase PHASE4 | Recurrent Depressive Disorder | COMPLETED | NCT02016261 |
| Fluvoxamine | Other | Phase PHASE4 | Recurrent Depressive Disorder | COMPLETED | NCT02016261 |
| Triage CardioProfilER (Troponin I, Myoglobin, CK-MB, BNP) | Other | Phase PHASE4 | Acute Coronary Syndrome | WITHDRAWN | NCT00206817 |
| Reference Group | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02322138 |
| Experimental 2 Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02322138 |
| Experimental 1 Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02322138 |
| Triage BNP Test | Other | Approved | Heart Failure | COMPLETED | NCT00206843 |
| Triage Profiler S.O.B. Panel | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT00206830 |
| XIENCE PRIME SV EECSS | Other | Approved | Vascular Disease | COMPLETED | NCT01115933 |
| Standard nutritional supplement | Other | Phase PHASE4 | Hip Fractures | TERMINATED | NCT01850251 |
| Supplement with HMB and vitamin D | Other | Phase PHASE4 | Hip Fractures | TERMINATED | NCT01850251 |
| Standard nutritional supplement | Other | Phase PHASE4 | Hip Fractures | TERMINATED | NCT01850251 |
| Supplement with HMB and vitamin D | Other | Phase PHASE4 | Hip Fractures | TERMINATED | NCT01850251 |
| Lopinavir/ritonavir simplification strategy | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00159224 |
| Lopinavir/ritonavir simplification strategy | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00159224 |
| Lopinavir/ritonavir simplification strategy | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00159224 |
| Administration of patient self-assessment | Other | Preclinical | Cataract | COMPLETED | NCT02146599 |
| RevitaLens OcuTec MPS (Investigational MPS) and Opti-Free RepleniSH MPS (control) | Other | Phase PHASE1 | Myopia | COMPLETED | NCT01024855 |
| Xience | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT01350869 |
| Xience | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT01350869 |
| Placebo | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| Adalimumab | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| Placebo | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| Adalimumab | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| Placebo | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| Adalimumab | Other | Phase PHASE3 | Arthritis, Rheumatoid | COMPLETED | NCT00660647 |
| SMBG and CGM | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01072565 |
| SMBG to guide clinical decisions | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01072565 |
| SMBG and CGM | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01072565 |
| SMBG to guide clinical decisions | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01072565 |
| Preterm infant formula per standard of care | Other | Preclinical | Other Preterm Infants | COMPLETED | NCT02073071 |
| Continuous Glucose Monitoring of Carbohydrate Intake | Other | Preclinical | Type 2 Diabetes | COMPLETED | NCT00818077 |
| Continuous Glucose Monitoring of Carbohydrate Intake | Other | Preclinical | Type 2 Diabetes | COMPLETED | NCT00818077 |
| CGM System for Type 1 and Type 2 Diabetes Mellitus | Other | Preclinical | NonDiabetes | COMPLETED | NCT00467675 |
| Point of care lactate measurement | Other | Preclinical | Sepsis | COMPLETED | NCT02189096 |
| NEWS and Sepsis Screening | Other | Preclinical | Sepsis | COMPLETED | NCT02189096 |
| iDesign® Advanced WaveScan Studio | Other | Phase PHASE3 | Keratoconus | UNKNOWN | NCT02613780 |
| Photorefractive keratectomy | Other | Phase PHASE3 | Keratoconus | UNKNOWN | NCT02613780 |
| Crosslinking | Other | Phase PHASE3 | Keratoconus | UNKNOWN | NCT02613780 |
| Juven | Other | Phase PHASE1 | Pressure Ulcers | TERMINATED | NCT00502372 |
| Nutritional Supplement/Amino acids and HMB | Other | Phase PHASE1 | Pressure Ulcers | TERMINATED | NCT00502372 |
| Juven | Other | Phase PHASE1 | Pressure Ulcers | TERMINATED | NCT00502372 |
| Nutritional Supplement/Amino acids and HMB | Other | Phase PHASE1 | Pressure Ulcers | TERMINATED | NCT00502372 |
| Amiodarone | Other | Approved | Atrial Fibrillation | TERMINATED | NCT01276093 |
| PVI ablation | Other | Approved | Atrial Fibrillation | TERMINATED | NCT01276093 |
| Phase 2- Arm 3 Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02401217 |
| Phase 2- Arm 2 Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02401217 |
| Phase 1- Arm 1 Infant Formula | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02401217 |
| Nutritional beverage fortified with 12mg lutein/day | Other | Phase PHASE2 | Healthy But Chronically Stressed | COMPLETED | NCT02257801 |
| Nutritional beverage fortified with 6mg lutein/day | Other | Phase PHASE2 | Healthy But Chronically Stressed | COMPLETED | NCT02257801 |
| Creon N | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | COMPLETED | NCT02137382 |
| Creon® | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | COMPLETED | NCT02137382 |
| Creon N | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | COMPLETED | NCT02137382 |
| Creon® | Other | Phase PHASE3 | Pancreatic Exocrine Insufficiency Due to Cystic Fibrosis | COMPLETED | NCT02137382 |
| VSS-Rx1 OPM vs Commercial iDesign Treatment | Drug | Approved | Myopia | COMPLETED | NCT01988415 |
| divalproex sodium | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00287053 |
| divalproex sodium | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00287053 |
| SAMe 2000 mg | Other | Phase PHASE3 | Non Alcoholic Fatty Liver Disease | COMPLETED | NCT01754714 |
| SAMe 1500 mg | Other | Phase PHASE3 | Non Alcoholic Fatty Liver Disease | COMPLETED | NCT01754714 |
| SAMe 1000 mg | Other | Phase PHASE3 | Non Alcoholic Fatty Liver Disease | COMPLETED | NCT01754714 |
| Usual Nutrition Care | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| MNT according to AND EBNPG for Type 2 DM | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| Usual Nutrition Care | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| MNT according to AND EBNPG for Type 2 DM | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| Usual Nutrition Care | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| MNT according to AND EBNPG for Type 2 DM | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| Usual Nutrition Care | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| MNT according to AND EBNPG for Type 2 DM | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT01703611 |
| ER Niacin | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| ABT335 | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| Atorvastatin | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| ER Niacin | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| ABT335 | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| Atorvastatin | Other | Phase PHASE2 | Dyslipidemia | COMPLETED | NCT00728910 |
| Standard SMBG | Other | Phase PHASE4 | Diabetes Mellitus | COMPLETED | NCT01713348 |
| FreeStyle Navigator | Other | Phase PHASE4 | Diabetes Mellitus | COMPLETED | NCT01713348 |
| FreeStyle Freedom Lite | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01519466 |
| FreeStyle InsuLinx | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01519466 |
| FreeStyle Freedom Lite | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01519466 |
| FreeStyle InsuLinx | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01519466 |
| Creon® (DR/GR) | Other | Phase PHASE2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | COMPLETED | NCT02415959 |
| Creon IR | Other | Phase PHASE2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | COMPLETED | NCT02415959 |
| Creon® (DR/GR) | Other | Phase PHASE2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | COMPLETED | NCT02415959 |
| Creon IR | Other | Phase PHASE2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | COMPLETED | NCT02415959 |
| Simvastatin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| Extended release niacin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| Simvastatin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| Extended release niacin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| Simvastatin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| Extended release niacin | Other | Phase PHASE3 | Cardiovascular Diseases | TERMINATED | NCT00120289 |
| SCS Alone | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01990287 |
| SCS and PNfS | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01990287 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | TERMINATED | NCT01562951 |
| ADALIMUMAB | Other | Phase PHASE3 | Crohn's Disease | TERMINATED | NCT01562951 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | TERMINATED | NCT01562951 |
| ADALIMUMAB | Other | Phase PHASE3 | Crohn's Disease | TERMINATED | NCT01562951 |
| Implantation procedure for a St-Jude Medical pacemaker system with left ventricular apex pacing | Procedure | Approved | Bradyarrhythmia | TERMINATED | NCT01535404 |
| Implantation procedure for a St-Jude Medical pacemaker system with right ventricular apex pacing | Procedure | Approved | Bradyarrhythmia | TERMINATED | NCT01535404 |
| Resting conditions | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02184117 |
| Contrast Media | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02184117 |
| Adenosine | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02184117 |
| Maternal Nutritional Supplement | Other | Approved | Breast Feeding | COMPLETED | NCT02016586 |
| Maternal Nutritional Supplement | Other | Approved | Breast Feeding | COMPLETED | NCT02016586 |
| Low-Na high-CHO beverage | Other | Approved | Dehydration Related to Exercise | COMPLETED | NCT01974986 |
| High-Na low-CHO beverage | Other | Approved | Dehydration Related to Exercise | COMPLETED | NCT01974986 |
| Water with flavoring and non-nutritive sweetener. | Other | Approved | Dehydration Related to Exercise | COMPLETED | NCT01974986 |
| Control protein powder sachet | Other | Approved | Malnutrition | COMPLETED | NCT02052232 |
| Experimental protein powder sachet | Other | Approved | Malnutrition | COMPLETED | NCT02052232 |
| XIENCE V® EECSS | Other | Phase PHASE4 | Coronary Disease | COMPLETED | NCT01171820 |
| TAXUS® Liberté™ | Other | Phase PHASE4 | Coronary Disease | COMPLETED | NCT01171820 |
| XIENCE V® EECSS | Other | Phase PHASE4 | Coronary Disease | COMPLETED | NCT01171820 |
| TAXUS® Liberté™ | Other | Phase PHASE4 | Coronary Disease | COMPLETED | NCT01171820 |
| Capsule endoscopy | Other | Phase PHASE4 | Plaque Psoriasis | COMPLETED | NCT01556672 |
| Adalimumab | Other | Phase PHASE4 | Plaque Psoriasis | COMPLETED | NCT01556672 |
| Capsule endoscopy | Other | Phase PHASE4 | Plaque Psoriasis | COMPLETED | NCT01556672 |
| Adalimumab | Other | Phase PHASE4 | Plaque Psoriasis | COMPLETED | NCT01556672 |
| ONS containing AN777 | Other | Approved | Healthy | COMPLETED | NCT02090387 |
| ONS without AN777 | Other | Approved | Healthy | COMPLETED | NCT02090387 |
| Escalated Antiarrhythmic Therapy | Drug | Phase PHASE4 | Recurrent Ventricular Tachycardia | COMPLETED | NCT00905853 |
| Catheter Ablation | Other | Phase PHASE4 | Recurrent Ventricular Tachycardia | COMPLETED | NCT00905853 |
| Escalated Antiarrhythmic Therapy | Drug | Phase PHASE4 | Recurrent Ventricular Tachycardia | COMPLETED | NCT00905853 |
| Catheter Ablation | Other | Phase PHASE4 | Recurrent Ventricular Tachycardia | COMPLETED | NCT00905853 |
| Control Study Product | Other | Approved | Diabetes | WITHDRAWN | NCT01850134 |
| Experimental Study Product | Other | Approved | Diabetes | WITHDRAWN | NCT01850134 |
| Alpine | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT02845804 |
| Alpine | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT02845804 |
| Tecnis Multifocal 1-Piece IOL | Other | Approved | Cataract | UNKNOWN | NCT02863159 |
| Tecnis Multifocal 1-Piece IOL | Other | Approved | Cataract | UNKNOWN | NCT02863159 |
| clarithromycin | Other | Phase PHASE3 | Heart Disease | COMPLETED | NCT00121550 |
| clarithromycin | Other | Phase PHASE3 | Heart Disease | COMPLETED | NCT00121550 |
| CYPHER SELECT PLUS SECSS | Other | Phase PHASE4 | Coronary Occlusion | COMPLETED | NCT01178268 |
| XIENCE V EECSS | Other | Phase PHASE4 | Coronary Occlusion | COMPLETED | NCT01178268 |
| CYPHER SELECT PLUS SECSS | Other | Phase PHASE4 | Coronary Occlusion | COMPLETED | NCT01178268 |
| XIENCE V EECSS | Other | Phase PHASE4 | Coronary Occlusion | COMPLETED | NCT01178268 |
| placebo | Other | Phase PHASE4 | Dyslipidemia | TERMINATED | NCT01025492 |
| Trilipix | Other | Phase PHASE4 | Dyslipidemia | TERMINATED | NCT01025492 |
| Placebo | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01722214 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01722214 |
| Placebo | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01722214 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01722214 |
| FreeStyle Precision Neo-Meter | Other | Approved | Type 2 Diabetes | COMPLETED | NCT02553408 |
| FreeStyle Precision Neo-Meter | Other | Approved | Type 2 Diabetes | COMPLETED | NCT02553408 |
| Adalimumab | Other | Phase PHASE4 | Spondyloarthritis | WITHDRAWN | NCT00972218 |
| FreeStyle Libre Pro 3 sensor wears | Other | Approved | Diabetes Mellitus | COMPLETED | NCT02434315 |
| FreeStyle Libre Pro 6 sensor wears, 4 with reviews | Other | Approved | Diabetes Mellitus | COMPLETED | NCT02434315 |
| FreeStyle Libre Pro 4 sensor wears, 2 with reviews | Other | Approved | Diabetes Mellitus | COMPLETED | NCT02434315 |
| EnligHTN™ Renal Denervation System | Other | Phase PHASE1 | Chronic Heart Failure | UNKNOWN | NCT02471729 |
| Adalimumab (Humira) | Other | Phase PHASE3 | Arthritis; Behcet | COMPLETED | NCT01497717 |
| Adalimumab (Humira) | Other | Phase PHASE3 | Arthritis; Behcet | COMPLETED | NCT01497717 |
| Adalimumab | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT00814866 |
| Adalimumab | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT00814866 |
| Adalimumab | Other | Approved | Rheumatoid Arthritis | COMPLETED | NCT00814866 |
| Echo | Other | Phase PHASE4 | Tricuspid Regurgitation | COMPLETED | NCT01093001 |
| Placebo | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00481013 |
| Valproic Acid (VPA) | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00481013 |
| Placebo | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00481013 |
| Valproic Acid (VPA) | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00481013 |
| FAST Carbohydrate | Other | Approved | Cognitive Ability, General | COMPLETED | NCT02630667 |
| MEDIUM Carbohydrate | Other | Approved | Cognitive Ability, General | COMPLETED | NCT02630667 |
| SLOW Carbohydrate | Other | Approved | Cognitive Ability, General | COMPLETED | NCT02630667 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT02381418 |
| Trivalent influenza subunit vaccine Influvac | Other | Phase PHASE3 | Influenza | COMPLETED | NCT02381418 |
| Placebo | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00413244 |
| AndroGel 5 Grams | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00413244 |
| Placebo | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00413244 |
| AndroGel 5 Grams | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00413244 |
| paricalcitol | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00796679 |
| paricalcitol | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT00796679 |
| TECNIS Monofocal IOL, Model ZCB00 | Other | Approved | Cataract | COMPLETED | NCT02203721 |
| TECNIS Symfony Extended Range of Vision IOL, Model ZXR00 | Other | Approved | Cataract | COMPLETED | NCT02203721 |
| TECNIS Monofocal IOL, Model ZCB00 | Other | Approved | Cataract | COMPLETED | NCT02203721 |
| TECNIS Symfony Extended Range of Vision IOL, Model ZXR00 | Other | Approved | Cataract | COMPLETED | NCT02203721 |
| Weight Loss | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Fenofibrate | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Rosiglitazone | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Weight Loss | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Fenofibrate | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Rosiglitazone | Other | Approved | Insulin Resistance | COMPLETED | NCT00186537 |
| Abbott Sensor Based Glucose Monitoring System-Professional | Other | Preclinical | Type 2 Diabetes Mellitus | COMPLETED | NCT02336945 |
| No treatment | Drug | Preclinical | Type2 Diabetes | COMPLETED | NCT01932944 |
| Fenofibrate (drug) | Drug | Approved | Hypertriglyceridemia With the Metabolic Syndrome | COMPLETED | NCT00422396 |
| Fenofibrate (drug) | Drug | Approved | Hypertriglyceridemia With the Metabolic Syndrome | COMPLETED | NCT00422396 |
| Nutritional Supplement (Ensure Plus) | Other | Approved | Malnutrition | WITHDRAWN | NCT01190969 |
| Nutritional Supplement (Ensure Plus) | Other | Approved | Malnutrition | WITHDRAWN | NCT01190969 |
| Fractional Flow Reserve Measurement | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT03055910 |
| MITRACLIP | Other | Phase PHASE4 | MITRAL REGURGITATION | UNKNOWN | NCT02592889 |
| MITRACLIP | Other | Phase PHASE4 | MITRAL REGURGITATION | UNKNOWN | NCT02592889 |
| Collection of cervical sample for routine cervical screening | Other | Approved | Cervix Diseases | WITHDRAWN | NCT02779621 |
| Self-collecting a vaginal sample with a swab for HPV testing | Other | Approved | Cervix Diseases | WITHDRAWN | NCT02779621 |
| Collection of cervical sample for routine cervical screening | Other | Approved | Cervix Diseases | WITHDRAWN | NCT02779621 |
| Self-collecting a vaginal sample with a swab for HPV testing | Other | Approved | Cervix Diseases | WITHDRAWN | NCT02779621 |
| percutaneous coronary intervention | Other | Phase PHASE4 | Coronary Artery Disease | TERMINATED | NCT01489761 |
| placebo | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT01393808 |
| Paricalcitol | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT01393808 |
| placebo | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT01393808 |
| Paricalcitol | Other | Phase PHASE2 | Type 2 Diabetes | COMPLETED | NCT01393808 |
| Opti-Free RepleniSH | Other | Approved | Normal Contact Lens Wearers | COMPLETED | NCT01294917 |
| Clear Care | Other | Approved | Normal Contact Lens Wearers | COMPLETED | NCT01294917 |
| Multi-purpose disinfecting solution | Other | Approved | Normal Contact Lens Wearers | COMPLETED | NCT01294917 |
| Metformin and Fenofibrate placebo | Other | Phase PHASE2 | Metabolic Syndrome x | COMPLETED | NCT00400231 |
| Study Drug: fenofibrate | Drug | Phase PHASE2 | Metabolic Syndrome x | COMPLETED | NCT00400231 |
| Study Drug: Metformin | Drug | Phase PHASE2 | Metabolic Syndrome x | COMPLETED | NCT00400231 |
| Study drugs: Metformin and fenofibrate | Drug | Phase PHASE2 | Metabolic Syndrome x | COMPLETED | NCT00400231 |
| Placebo | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Cholecalciferol | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Paricalcitol | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Placebo | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Cholecalciferol | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Paricalcitol | Other | Phase PHASE3 | Gastric Bypass | COMPLETED | NCT01138475 |
| Nutrition Products | Other | Approved | Healthy | COMPLETED | NCT02732158 |
| Milk based standard infant formula | Other | Approved | Infant Newborn | COMPLETED | NCT01300000 |
| Investigational infant formula | Other | Approved | Infant Newborn | COMPLETED | NCT01300000 |
| Human Milk | Other | Approved | Infant Newborn | COMPLETED | NCT01300000 |
| Infant Formula supplemented with Oligosaccharides | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02746016 |
| Infant Formula supplemented with Oligosaccharides | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT02746016 |
| Placebo | Other | Phase PHASE4 | Nocturnal Hypokinesia | UNKNOWN | NCT03098368 |
| Rotigotine | Other | Phase PHASE4 | Nocturnal Hypokinesia | UNKNOWN | NCT03098368 |
| Placebo | Other | Phase PHASE4 | Nocturnal Hypokinesia | UNKNOWN | NCT03098368 |
| Rotigotine | Other | Phase PHASE4 | Nocturnal Hypokinesia | UNKNOWN | NCT03098368 |
| Pressure-wire guided CRT implant | Other | Phase PHASE2 | Heart Failure | UNKNOWN | NCT01464502 |
| Standard CRT Implant | Other | Phase PHASE2 | Heart Failure | UNKNOWN | NCT01464502 |
| Education and Feedback | Other | Approved | SpA | COMPLETED | NCT01749618 |
| Education and Feedback | Other | Approved | SpA | COMPLETED | NCT01749618 |
| Education and Feedback | Other | Approved | SpA | COMPLETED | NCT01749618 |
| Standard Blood Glucose Monitoring | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT02232698 |
| Sensor Based Glucose Monitoring System | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT02232698 |
| Depakote ER | Other | Phase PHASE4 | Depression, Bipolar | COMPLETED | NCT00186186 |
| Depakote ER | Other | Phase PHASE4 | Depression, Bipolar | COMPLETED | NCT00186186 |
| Diabetes specific ONS 2 | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| Diabetes specific ONS 1 | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| Standard ONS | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| Diabetes specific ONS 2 | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| Diabetes specific ONS 1 | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| Standard ONS | Other | Approved | Diabetes | COMPLETED | NCT02923960 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Approved | Diabetes Mellitus | COMPLETED | NCT02821117 |
| Seroquel | Other | Phase PHASE3 | Agitation | TERMINATED | NCT00315900 |
| Depakote ER | Other | Phase PHASE3 | Agitation | TERMINATED | NCT00315900 |
| Seroquel | Other | Phase PHASE3 | Agitation | TERMINATED | NCT00315900 |
| Depakote ER | Other | Phase PHASE3 | Agitation | TERMINATED | NCT00315900 |
| euglycemic and hypoglycemic clamp | Other | Approved | Hypoglycemia | COMPLETED | NCT01283126 |
| Human Milk Fortifier B | Other | Approved | Infant Growth | COMPLETED | NCT02307760 |
| Human Milk Fortifier A | Other | Approved | Infant Growth | COMPLETED | NCT02307760 |
| Clarithromycin | Other | Phase PHASE4 | Nontuberculous Mycobacteria | COMPLETED | NCT00600769 |
| Clarithromycin | Other | Phase PHASE4 | Nontuberculous Mycobacteria | COMPLETED | NCT00600769 |
| clarithromycin, rifabutin | Other | Phase PHASE4 | Mycobacterium Avium Complex Lung Disease | COMPLETED | NCT00598897 |
| clarithromycin, rifabutin | Other | Phase PHASE4 | Mycobacterium Avium Complex Lung Disease | COMPLETED | NCT00598897 |
| clarithromycin, rifabutin | Other | Phase PHASE4 | Mycobacterium Avium Complex Lung Disease | COMPLETED | NCT00598897 |
| Standard Blood Glucose Monitoring | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT02082184 |
| Sensor Based Glucose Monitoring System | Other | Approved | Type 2 Diabetes Mellitus | COMPLETED | NCT02082184 |
| Placebo | Other | Phase PHASE3 | Liver Disease, Alcoholic | COMPLETED | NCT00573313 |
| S-adenosylmethionine | Other | Phase PHASE3 | Liver Disease, Alcoholic | COMPLETED | NCT00573313 |
| Angioseal closure device | Device | Approved | Coronary Disease | COMPLETED | NCT02234830 |
| Exoseal closure device | Device | Approved | Coronary Disease | COMPLETED | NCT02234830 |
| Angioseal closure device | Device | Approved | Coronary Disease | COMPLETED | NCT02234830 |
| Exoseal closure device | Device | Approved | Coronary Disease | COMPLETED | NCT02234830 |
| Stenting using Absolute Pro® and Pro LL® Peripheral Stent Systems | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT01444378 |
| Placebo | Other | Phase PHASE4 | Photosensitive Epilepsy | COMPLETED | NCT00609245 |
| Valproic Acid | Other | Phase PHASE4 | Photosensitive Epilepsy | COMPLETED | NCT00609245 |
| Placebo | Other | Phase PHASE4 | Photosensitive Epilepsy | COMPLETED | NCT00609245 |
| Valproic Acid | Other | Phase PHASE4 | Photosensitive Epilepsy | COMPLETED | NCT00609245 |
| Conventional biochemical and clinical examinations | Other | Approved | Arthritis | COMPLETED | NCT01656278 |
| Magnetic resonance imaging (MRI) | Other | Approved | Arthritis | COMPLETED | NCT01656278 |
| Conventional biochemical and clinical examinations | Other | Approved | Arthritis | COMPLETED | NCT01656278 |
| Magnetic resonance imaging (MRI) | Other | Approved | Arthritis | COMPLETED | NCT01656278 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03141892 |
| Placebo | Other | Approved | Heart Failure | WITHDRAWN | NCT01377103 |
| testerone gel | Other | Approved | Heart Failure | WITHDRAWN | NCT01377103 |
| Placebo | Other | Approved | Heart Failure | WITHDRAWN | NCT01377103 |
| testerone gel | Other | Approved | Heart Failure | WITHDRAWN | NCT01377103 |
| Carotid artery endarterectomy (surgical) | Other | Approved | Carotid Artery Disease | TERMINATED | NCT00106938 |
| Carotid artery stenting with filter (interventional) | Other | Approved | Carotid Artery Disease | TERMINATED | NCT00106938 |
| Cataract Surgery | Procedure | Approved | Cataract | COMPLETED | NCT02847572 |
| Cataract Surgery | Procedure | Approved | Cataract | COMPLETED | NCT02847572 |
| Nutritional Study Product | Other | Approved | Malabsorption | COMPLETED | NCT02750787 |
| Nutritional Study Product | Other | Approved | Malabsorption | COMPLETED | NCT02750787 |
| ADC blood glucose meter with insulin calculator active | Other | Approved | Diabetes Mellitus | COMPLETED | NCT01432275 |
| Comparator blood glucose meter | Other | Approved | Diabetes Mellitus | COMPLETED | NCT01432275 |
| ADC blood glucose meter | Other | Approved | Diabetes Mellitus | COMPLETED | NCT01432275 |
| Lifestyle intervention | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT03249610 |
| Oral Nutritional Supplement (ONS) | Other | Approved | Chronic Kidney Disease | COMPLETED | NCT02046746 |
| CHO Experimental 4 Maltodextrin | Other | Approved | Glycemic Index | COMPLETED | NCT03242122 |
| CHO Experimental 3 Low Sugar | Other | Approved | Glycemic Index | COMPLETED | NCT03242122 |
| CHO Experimental 2 Digestion Resistant | Other | Approved | Glycemic Index | COMPLETED | NCT03242122 |
| CHO Experimental 1 Slowly Digested | Other | Approved | Glycemic Index | COMPLETED | NCT03242122 |
| CHO Control 1 and 2 Glucose | Other | Approved | Glycemic Index | COMPLETED | NCT03242122 |
| Device: FreeStyle Libre Flash Glucose Monitoring System | Device | Preclinical | Diabete Mellitus | COMPLETED | NCT03159546 |
| HERMES tablet | Other | Preclinical | Mitral Regurgitation | UNKNOWN | NCT02698150 |
| Implantable Cardioverter Defibrillator (ICD) | Other | Approved | Ventricular Tachycardia | WITHDRAWN | NCT02844127 |
| SUPERA Interwoven self-expanding nitinol stent | Other | Approved | Peripheral Artery Disease | TERMINATED | NCT01154751 |
| SUPERA Interwoven self-expanding nitinol stent | Other | Approved | Peripheral Artery Disease | TERMINATED | NCT01154751 |
| ABT-888/Bortezomib | Other | Phase PHASE1 | Multiple Myeloma | COMPLETED | NCT01495351 |
| ABT-888/Bortezomib | Other | Phase PHASE1 | Multiple Myeloma | COMPLETED | NCT01495351 |
| ABT-888/Bortezomib | Other | Phase PHASE1 | Multiple Myeloma | COMPLETED | NCT01495351 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | TERMINATED | NCT02150473 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | TERMINATED | NCT02150473 |
| placebo | Other | Phase PHASE4 | Gait or Balance Disorder Problems | COMPLETED | NCT01468285 |
| betahistine dihydrochloride | Other | Phase PHASE4 | Gait or Balance Disorder Problems | COMPLETED | NCT01468285 |
| Frequency domain optical coherence tomography | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT03058510 |
| Frequency domain optical coherence tomography | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT03058510 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Calcitriol (Rocaltrol®) | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Calcitriol (Rocaltrol®) | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Paricalcitol | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Calcitriol (Rocaltrol®) | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT00752102 |
| Placebo | Other | Phase PHASE3 | Disorder of Transplanted Kidney | COMPLETED | NCT01436747 |
| Paricalcitol | Other | Phase PHASE3 | Disorder of Transplanted Kidney | COMPLETED | NCT01436747 |
| Placebo | Other | Phase PHASE3 | Disorder of Transplanted Kidney | COMPLETED | NCT01436747 |
| Paricalcitol | Other | Phase PHASE3 | Disorder of Transplanted Kidney | COMPLETED | NCT01436747 |
| Placebo dydrogesterone | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Placebo progesterone | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Micronized Progesterone 600 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Dydrogesterone 30 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Placebo dydrogesterone | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Placebo progesterone | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Micronized Progesterone 600 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| Dydrogesterone 30 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT01850030 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03257501 |
| Absorb BVS | Other | Approved | Ischemic Heart Disease | WITHDRAWN | NCT02943616 |
| Placebo and tube feed | Other | Approved | Gastrointestinal Hemorrhage | COMPLETED | NCT01477320 |
| Pantoprazole 40 mg IV daily and tube feed. | Other | Approved | Gastrointestinal Hemorrhage | COMPLETED | NCT01477320 |
| ABSORB BVS | Other | Approved | Myocardial Ischemia | UNKNOWN | NCT02928198 |
| ABSORB BVS | Other | Approved | Myocardial Ischemia | UNKNOWN | NCT02928198 |
| paricalcitol | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT00064376 |
| paricalcitol | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT00064376 |
| Divalproex Sodium Extended-Release Tablets | Other | Approved | Elderly | COMPLETED | NCT00318929 |
| Divalproex Sodium Extended-Release Tablets | Other | Approved | Elderly | COMPLETED | NCT00318929 |
| Point of Care cTnL testing | Other | Preclinical | Angina, Unstable | COMPLETED | NCT00222352 |
| Point of Care cTnL testing | Other | Preclinical | Angina, Unstable | COMPLETED | NCT00222352 |
| Transthoracic Echocardiogram (TTE) Assesment | Other | Approved | Acute Heart Failure | COMPLETED | NCT02728739 |
| ABSORB BVS | Other | Approved | Myocardial Ischemia | COMPLETED | NCT01023789 |
| Placebo | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01014741 |
| Ibutilide | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01014741 |
| Placebo | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01014741 |
| Ibutilide | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01014741 |
| XIENCE V / PROMUS stent | Other | Preclinical | Angina | COMPLETED | NCT01086228 |
| XIENCE V / PROMUS stent | Other | Preclinical | Angina | COMPLETED | NCT01086228 |
| Placebo | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Divalproex | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Lithium | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Placebo | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Divalproex | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Lithium | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194129 |
| Abbott Sensor Based Glucose Monitoring System | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT02283411 |
| Abbott Sensor Based Glucose Monitoring System | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT02283411 |
| Placebo | Other | Phase PHASE3 | Allergy | COMPLETED | NCT02596321 |
| Mitizax | Other | Phase PHASE3 | Allergy | COMPLETED | NCT02596321 |
| Stent delivery with Alpine | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Stent delivery with Xpedition | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Stent delivery with Alpine | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Stent delivery with Xpedition | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Stent delivery with Alpine | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Stent delivery with Xpedition | Other | Approved | Percutaneous Coronary Intervention | UNKNOWN | NCT03451617 |
| Freestyle Navigator | Other | Approved | Critical Illness | COMPLETED | NCT00694473 |
| Metformin | Other | Phase PHASE1 | Polycystic Ovary Syndrome | COMPLETED | NCT02086526 |
| Self-Regulatory Approaches | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00941447 |
| Physical Activity | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00941447 |
| Dietary | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00941447 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01609205 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01609205 |
| MEMS cap monitoring | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00785616 |
| MEMS cap monitoring | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00785616 |
| MEMS cap monitoring | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00785616 |
| AT LISA tri 839MP IOL | Other | Approved | Cataract | COMPLETED | NCT03117426 |
| SYMFONY IOL | Other | Approved | Cataract | COMPLETED | NCT03117426 |
| No intervention - registry | Other | Preclinical | Mitral Regurgitation | TERMINATED | NCT02858245 |
| No intervention - registry | Other | Preclinical | Mitral Regurgitation | TERMINATED | NCT02858245 |
| Fructooligosaccharide | Other | Phase PHASE1 | Osteoporosis | COMPLETED | NCT01005927 |
| CTO Treatment Device | Drug | Approved | Coronary Artery Disease (CAD) | COMPLETED | NCT01435031 |
| Experimental Nutritional Product | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Control Meal 2 | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Control Meal 1 | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Experimental Nutritional Product | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Control Meal 2 | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Control Meal 1 | Other | Approved | Glycemic Index | COMPLETED | NCT03508154 |
| Life Stent | Other | Approved | Femoropopliteal Stenosis | WITHDRAWN | NCT01643746 |
| Supera Stent | Other | Approved | Femoropopliteal Stenosis | WITHDRAWN | NCT01643746 |
| Percutaneous Coronary Intervention | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | COMPLETED | NCT01986803 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabete Mellitus | COMPLETED | NCT03369899 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabete Mellitus | COMPLETED | NCT03369899 |
| Treatment and education program for patients with diabetes who use flash glucose monitoring (FLASH) | Drug | Approved | Diabetes Mellitus | COMPLETED | NCT03175315 |
| Biaxin ( clarithromycin) | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT00205634 |
| Biaxin ( clarithromycin) | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT00205634 |
| Biaxin ( clarithromycin) | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT00205634 |
| Nutritional Supplement | Other | Preclinical | Malnutrition | COMPLETED | NCT02698540 |
| Nutritional Supplement | Other | Preclinical | Malnutrition | COMPLETED | NCT02698540 |
| Implantable Cardiac Monitor (Confirm ICM model 2102) | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT01694394 |
| Implantable Cardiac Monitor (Confirm ICM model 2102) | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT01694394 |
| IntraVascular UltraSound | Other | Approved | Coronary Artery Disease | TERMINATED | NCT02814578 |
| Optical coherent tomography | Other | Approved | Coronary Artery Disease | TERMINATED | NCT02814578 |
| IntraVascular UltraSound | Other | Approved | Coronary Artery Disease | TERMINATED | NCT02814578 |
| Optical coherent tomography | Other | Approved | Coronary Artery Disease | TERMINATED | NCT02814578 |
| AMO phacoemulsification equipment | Other | Approved | Cataract Surgery | COMPLETED | NCT02910362 |
| Alcon phacoemulsification equipment | Other | Approved | Cataract Surgery | COMPLETED | NCT02910362 |
| AMO phacoemulsification equipment | Other | Approved | Cataract Surgery | COMPLETED | NCT02910362 |
| Alcon phacoemulsification equipment | Other | Approved | Cataract Surgery | COMPLETED | NCT02910362 |
| ABT-751 and Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Cancer | TERMINATED | NCT00735878 |
| Percutaneous mitral valve repair using MitraClip implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT01940120 |
| Percutaneous mitral valve repair using MitraClip implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT01940120 |
| MitraClip | Other | Approved | Cardiovascular Diseases | TERMINATED | NCT01772108 |
| MitraClip Implant | Other | Preclinical | Mitral Regurgitation | TERMINATED | NCT01301625 |
| MitraClip Implant | Other | Preclinical | Mitral Regurgitation | TERMINATED | NCT01301625 |
| MitraClip Implant | Other | Preclinical | Mitral Regurgitation | TERMINATED | NCT01301625 |
| Mitral Valve Surgery | Procedure | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| Medical Management | Other | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| MitraClip | Other | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| Mitral Valve Surgery | Procedure | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| Medical Management | Other | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| MitraClip | Other | Preclinical | Mitral Valve (MV) Regurgitation | COMPLETED | NCT01288976 |
| Mitral valve repair or replacement surgery | Procedure | Approved | Mitral Valve Insufficiency | COMPLETED | NCT00209274 |
| Percutaneous mitral valve repair using MitraClip implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT00209274 |
| Mitral valve repair or replacement surgery | Procedure | Approved | Mitral Valve Insufficiency | COMPLETED | NCT00209274 |
| Percutaneous mitral valve repair using MitraClip implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT00209274 |
| Control Infant Formula | Other | Approved | Growth | COMPLETED | NCT03276884 |
| Experimental Infant Formula | Other | Approved | Growth | COMPLETED | NCT03276884 |
| MitraClip® implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT01931956 |
| MitraClip® implant | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT01931956 |
| Hydrolysate Infant Formula 2 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT03628183 |
| Hydrolysate Infant Formula 1 | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT03628183 |
| Multicomponent Risk Factor Modification | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT03785418 |
| MitraClip implantation | Other | Approved | Mitral Regurgitation Functional | WITHDRAWN | NCT03503851 |
| MitraClip implantation | Other | Approved | Mitral Regurgitation Functional | WITHDRAWN | NCT03503851 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03502174 |
| Pulmonary Vein Isolation | Other | Approved | Persistent Atrial Fibrillation | UNKNOWN | NCT03811938 |
| Low voltage ablation | Other | Approved | Persistent Atrial Fibrillation | UNKNOWN | NCT03811938 |
| Pulmonary Vein Isolation | Other | Approved | Persistent Atrial Fibrillation | UNKNOWN | NCT03811938 |
| Low voltage ablation | Other | Approved | Persistent Atrial Fibrillation | UNKNOWN | NCT03811938 |
| Electrophysiology study | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT02131337 |
| Burst Stimulation | Other | Approved | Chronic Pain | COMPLETED | NCT02011893 |
| Tonic Stimulation | Other | Approved | Chronic Pain | COMPLETED | NCT02011893 |
| Placebo | Other | Approved | Diabetic Polyneuropathy | WITHDRAWN | NCT01536236 |
| ANS Eon™ Implantable Pulse Generator (Permanent Implant) | Other | Approved | Diabetic Polyneuropathy | WITHDRAWN | NCT01536236 |
| St. Jude Medical Spinal Cord Stimulation Systems | Other | Preclinical | Pain | COMPLETED | NCT01305525 |
| Occipital Stimulation | Other | Approved | Fibromyalgia | COMPLETED | NCT01298609 |
| Contact force assisted irrigated RF ablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01223469 |
| PVI + CFE ablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01203748 |
| PVI | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01203748 |
| PVI + Lines ablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01203748 |
| QuickOpt | Other | Approved | Heart Failure | COMPLETED | NCT00918294 |
| SJM Confirm | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00746564 |
| SJM Confirm | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00746564 |
| Combined approach for AF ablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00367757 |
| Substrate via CFAEs | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00367757 |
| Ablate AF triggers via PVI | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00367757 |
| EnSite™ HD Grid Catheter mapping system | Other | Approved | Non-paroxysmal Atrial Fibrillation | COMPLETED | NCT02656537 |
| ECG+IEGM | Other | Preclinical | Heart Failure | COMPLETED | NCT02814214 |
| ICD/CRT-D with NIPS or EP Study | Other | Preclinical | Monomorphic Ventricular Tachycardia | WITHDRAWN | NCT02584595 |
| Quartet 1457Q LV Lead | Other | Approved | Heart Failure | COMPLETED | NCT02548455 |
| VIP | Other | Approved | Sinus Node Disease | COMPLETED | NCT02485093 |
| Septal ventricular pacing | Other | Approved | Sinus Node Disease | COMPLETED | NCT02485093 |
| MediGuide | Other | Preclinical | Heart Failure | TERMINATED | NCT02470312 |
| CRT implantation | Other | Preclinical | Heart Failure | TERMINATED | NCT02470312 |
| Unpaired remote monitoring transmitter | Other | Phase PHASE4 | Heart Disease | WITHDRAWN | NCT02421549 |
| atrial septal occluder | Other | Preclinical | Atrial Septal Defect Secundum | TERMINATED | NCT02353351 |
| Implantation with the commercially available Axium Neurostimulator | Other | Preclinical | Chronic Pain | TERMINATED | NCT02346643 |
| QST Testing | Other | Preclinical | Post Surgical Groin Pain | TERMINATED | NCT02337699 |
| Implantation with the commercially available Axium neurostimulator | Other | Preclinical | Post Surgical Groin Pain | TERMINATED | NCT02337699 |
| Implantation with the commercially available Axium neurostimulator | Other | Preclinical | Chronic Pain | COMPLETED | NCT02335502 |
| Implantation with the commercially available Axium neurostimulator | Other | Preclinical | Chronic Neuropathic Pain | TERMINATED | NCT02335489 |
| Hemodynamic measurements for CRT device programming | Device | Approved | Heart Failure | COMPLETED | NCT02064751 |
| CRT with MultiPoint Pacing | Other | Approved | Heart Failure | COMPLETED | NCT02064751 |
| ECG continuous recording (Analyze ST) | Other | Approved | Brugada Syndrome | COMPLETED | NCT02052765 |
| ECG continuous recording (Analyze ST) | Other | Approved | Brugada Syndrome | COMPLETED | NCT02052765 |
| Same Day Discharge | Other | Approved | Heart Failure | COMPLETED | NCT01993862 |
| ICD with enhanced SVT discriminators | Other | Approved | Tachycardia | COMPLETED | NCT01963286 |
| ICD with enhanced SVT discriminators | Other | Approved | Tachycardia | COMPLETED | NCT01963286 |
| Amplatzer Cardiac Plug | Other | Preclinical | Atrial Fibrillation | WITHDRAWN | NCT01962051 |
| Amplatzer Cardiac Plug | Other | Preclinical | Atrial Fibrillation | WITHDRAWN | NCT01962051 |
| EnligHTN™ Renal Denervation System. | Other | Approved | Metabolic Syndrome | COMPLETED | NCT01911078 |
| Renal Denervation | Other | Approved | Metabolic Syndrome | COMPLETED | NCT01911078 |
| CRT device implant with MultiPoint Pacing | Device | Approved | Heart Failure | COMPLETED | NCT01856725 |
| Hemodynamic measurements for CRT device programming | Device | Approved | Heart Failure | COMPLETED | NCT01856725 |
| CRT device implant with MultiPoint Pacing | Device | Approved | Heart Failure | COMPLETED | NCT01856725 |
| Hemodynamic measurements for CRT device programming | Device | Approved | Heart Failure | COMPLETED | NCT01856725 |
| Pacemaker | Other | Approved | Ventricular Dysfunction | COMPLETED | NCT01842243 |
| Septal pacing | Other | Approved | Ventricular Dysfunction | COMPLETED | NCT01842243 |
| Apical pacing | Other | Approved | Ventricular Dysfunction | COMPLETED | NCT01842243 |
| EnligHTN™ Renal Artery Ablation Catheter | Other | Approved | Hypertension | COMPLETED | NCT01836146 |
| St Jude Medical EON mini rechargeable system | Other | Approved | Heart Failure | WITHDRAWN | NCT01820130 |
| St Jude Medical EON mini rechargeable system | Other | Approved | Heart Failure | WITHDRAWN | NCT01820130 |
| EnSite NavX System | Other | Approved | Congestive Heart Failure | COMPLETED | NCT01615835 |
| Eon-mini IPG (implantable pulse generator) | Other | Phase PHASE1 | Traumatic Brain Injury | COMPLETED | NCT01588691 |
| PMVr procedure (SJM Percutaneous Mitral Valve Repair (PMVr) | Procedure | Phase PHASE1 | Mitral Valve Prolapse | COMPLETED | NCT01500148 |
| Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Symptomatic Aortic Stenosis | COMPLETED | NCT01487330 |
| quadripolar LV lead (Quartet) | Other | Preclinical | Heart Failure | COMPLETED | NCT01484613 |
| ESPRIT BVS | Other | Approved | Atherosclerosis | COMPLETED | NCT01468974 |
| Angio-Seal VIP | Other | Approved | Patients Requiring a Diagnostic and/or Interventional Diagnostic Procedure | COMPLETED | NCT01393041 |
| Spinal cord stimulation system | Other | Phase PHASE2 | Systolic Heart Failure | COMPLETED | NCT01362725 |
| DFT Testing with a 50/50% tilt | Other | Approved | DFT Testing | COMPLETED | NCT01325922 |
| Right ventricular lead location | Other | Approved | Sinus-node Dysfunction | COMPLETED | NCT01294839 |
| Right ventricular lead location | Other | Approved | Sinus-node Dysfunction | COMPLETED | NCT01294839 |
| Implantation of an Accent MRI device | Device | Preclinical | Bradycardia | COMPLETED | NCT01258218 |
| Implantation of an Accent MRI device | Device | Preclinical | Bradycardia | COMPLETED | NCT01258218 |
| Device Implantation | Device | Approved | Heart Failure | COMPLETED | NCT00746135 |
| Device Implantation | Device | Approved | Heart Failure | COMPLETED | NCT00746135 |
| ICD/ CRT-D | Other | Preclinical | Shock | COMPLETED | NCT00743522 |
| HIFU AF Ablation | Other | Approved | Coronary Arteriosclerosis | TERMINATED | NCT00735722 |
| Trifecta aortic heart valve | Other | Approved | Aortic Valve Insufficiency | COMPLETED | NCT00727181 |
| mitral valve repair (SJM® Rigid Saddle Ring) | Other | Approved | Mitral Valve Insufficiency | COMPLETED | NCT00727012 |
| AMPLATZER Duct Occluder II | Other | Approved | Patent Ductus Arteriosus | COMPLETED | NCT00713700 |
| Best Medical Treatment | Drug | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT00652522 |
| AF ablation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT00652522 |
| ICD/CRT implant | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT00652522 |
| Biocor and Biocor Supra valves | Other | Approved | Aortic Valve Insufficiency | COMPLETED | NCT00636987 |
| AMPLATZER Muscular VSD Occluder | Other | Preclinical | Muscular | APPROVED_FOR_MARKETING | NCT00590382 |
| Device closure with the AMPLATZER Membranous VSD Occluder | Device | Preclinical | Membranous | NO_LONGER_AVAILABLE | NCT00583505 |
| Device closure with the AMPLATZER Membranous VSD Occluder | Device | Preclinical | Membranous | NO_LONGER_AVAILABLE | NCT00583505 |
| Device closure with the AMPLATZER PFO Occluder | Device | Preclinical | Patent Foramen Ovale | NO_LONGER_AVAILABLE | NCT00583401 |
| AMPLATZER Membranous VSD Occluder | Other | Phase PHASE1 | Membranous Ventricular Septal Defects | COMPLETED | NCT00578708 |
| AMPLATZER Membranous VSD Occluder | Other | Phase PHASE1 | Membranous Ventricular Septal Defects | COMPLETED | NCT00578708 |
| AMPLATZER Membranous VSD Occluder | Other | Phase PHASE1 | Membranous Ventricular Septal Defects | COMPLETED | NCT00578708 |
| EnSite NavX-Guided CRT implant | Other | Phase EARLY_PHASE1 | Heart Failure | WITHDRAWN | NCT00577187 |
| EnSite NavX-Guided CRT implant | Other | Phase EARLY_PHASE1 | Heart Failure | WITHDRAWN | NCT00577187 |
| ICD Implant + Patient Notifier turned ON | Other | Approved | Tachycardia, Ventricular | COMPLETED | NCT00559559 |
| ICD implant + Patient Notifier turned OFF | Other | Approved | Tachycardia, Ventricular | COMPLETED | NCT00559559 |
| ICD Implant + Patient Notifier turned ON | Other | Approved | Tachycardia, Ventricular | COMPLETED | NCT00559559 |
| ICD implant + Patient Notifier turned OFF | Other | Approved | Tachycardia, Ventricular | COMPLETED | NCT00559559 |
| Dynamic Substrate Mapping-guided ablation | Other | Phase PHASE1 | Ischemic Ventricular Tachycardia | TERMINATED | NCT00558857 |
| Libra Deep Brain Stimulation System | Other | Approved | Parkinson Disease | COMPLETED | NCT00552474 |
| AMPLATZER® PFO Occluder Device | Device | Phase PHASE2 | Migraine | TERMINATED | NCT00505570 |
| Left atrial catheter ablation guided by introducer using Non-steerable sheeth | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00469638 |
| Left atrial catheter ablation guided by introducer using Agilis sheeth | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00469638 |
| Cardiac Resynchronization Therapy-Defibrillator | Drug | Preclinical | Heart Failure | COMPLETED | NCT00453622 |
| Cardiac Resynchronization Therapy-Defibrillator | Drug | Preclinical | Heart Failure | COMPLETED | NCT00453622 |
| Pacemaker implantation with RA lead in RAA position | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00419640 |
| Pacemaker implantation with RA lead in LAS position | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00419640 |
| Pacemaker implantation with RA lead in RAA position | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00419640 |
| Pacemaker implantation with RA lead in LAS position | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00419640 |
| Ventricular Intrinsic Preference | Other | Approved | Arrhythmia | COMPLETED | NCT00366158 |
| Device: St. Jude Medical Victory dual-chamber pacemaker | Device | Approved | Arrhythmia | COMPLETED | NCT00366158 |
| Ventricular Intrinsic Preference | Other | Approved | Arrhythmia | COMPLETED | NCT00366158 |
| Device: St. Jude Medical Victory dual-chamber pacemaker | Device | Approved | Arrhythmia | COMPLETED | NCT00366158 |
| Tissue valve | Other | Phase PHASE4 | Aortic Valve Stenosis | COMPLETED | NCT00256165 |
| AF Suppression Pacing Algorithm | Other | Phase PHASE4 | Hypertension | COMPLETED | NCT00256152 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT00187265 |
| Autointrinsic Conduction Search Algorithm | Other | Phase PHASE4 | Arrhythmia | COMPLETED | NCT00187239 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT00187213 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT00187213 |
| Implantable Defibrillator (ICD) | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00187187 |
| Angio-Seal VIP 6 French (6F) and 8 French (8F) devices | Device | Preclinical | Vascular Closure | COMPLETED | NCT01858636 |
| SJM Confirm ICM | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT01673256 |
| St. Jude Medical renal artery ablation system: RF ablation generator (IBI 1500T11.5) and Renal artery ablation catheter (DS3D001, DS3D002) | Other | Approved | Hypertension | COMPLETED | NCT01438229 |
| Cardiac Resynchronization Therapy - Defibrillator (CRT-D) | Drug | Phase PHASE4 | Sudden Cardiac Death | COMPLETED | NCT00626093 |
| Cardiac catheter ablation with ICD/CRT-D | Other | Approved | Monomorphic Ventricular Tachycardia | TERMINATED | NCT02130765 |
| Sham | Other | Approved | Hypertension | TERMINATED | NCT01903187 |
| EnligHTN Renal Denervation | Other | Approved | Hypertension | TERMINATED | NCT01903187 |
| Unpaired remote monitoring transmitter | Other | Approved | Heart Disease | COMPLETED | NCT01871090 |
| Unpaired remote monitoring transmitter | Other | Approved | Heart Disease | COMPLETED | NCT01871090 |
| Quad Group | Other | Approved | Postoperative Cardiac Complication | COMPLETED | NCT01510652 |
| BiP Group | Other | Approved | Postoperative Cardiac Complication | COMPLETED | NCT01510652 |
| Therapy™ Cool Flex™ Irrigated Ablation System | Drug | Approved | Typical Atrial Flutter | COMPLETED | NCT01408485 |
| Treatment Arm | Drug | Phase PHASE3 | Typical Atrial Flutter | COMPLETED | NCT01401361 |
| Therapy Cool Path Duo | Drug | Phase PHASE3 | Typical Atrial Flutter | COMPLETED | NCT00984204 |
| Testing of the autocapture features of the device | Device | Approved | Heart Failure | COMPLETED | NCT00746356 |
| Surgical ablation of permanent AF | Other | Approved | Atrial Fibrillation | TERMINATED | NCT00519194 |
| Epicor LP Cardiac Ablation System | Other | Approved | Atrial Fibrillation | TERMINATED | NCT00519194 |
| Trifecta Aortic Heart Valve | Other | Approved | Aortic Valve Insufficiency | COMPLETED | NCT00475709 |
| Trifecta Aortic Heart Valve | Other | Approved | Aortic Valve Insufficiency | COMPLETED | NCT00475709 |
| QuickOpt | Other | Approved | Cardiac Arrhythmias | COMPLETED | NCT00418314 |
| Control | Other | Approved | Cardiac Arrhythmias | COMPLETED | NCT00418314 |
| Cardiac Resynchronization Therapy Defibrillator | Drug | Phase PHASE4 | Heart Failure | COMPLETED | NCT01295840 |
| Implantable Cardioverter Defibrillator (ICD), Cardiac Resynchronization Therapy (CRT-D) | Drug | Phase PHASE4 | Sudden Cardiac Death | COMPLETED | NCT00311181 |
| Implantable Cardioverter Defibrillator (ICD), Cardiac Resynchronization Therapy (CRT-D) | Drug | Phase PHASE4 | Sudden Cardiac Death | COMPLETED | NCT00311181 |
| Catheter ablation to treat paroxysmal atrial fibrillation | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01278953 |
| Placebo | Other | Phase PHASE3 | Andropause | COMPLETED | NCT00799617 |
| AndroGel® (testosterone gel) | Other | Phase PHASE3 | Andropause | COMPLETED | NCT00799617 |
| Placebo | Other | Phase PHASE3 | Andropause | COMPLETED | NCT00799617 |
| AndroGel® (testosterone gel) | Other | Phase PHASE3 | Andropause | COMPLETED | NCT00799617 |
| FDA approved Open Irrigated RF Ablation System | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01056328 |
| SJM Irrigated Cardiac Ablation System | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01056328 |
| Artificial Mechanical Heart Valve | Other | Approved | Aortic Valve Disease | TERMINATED | NCT00590889 |
| XIENCE V® Everolimus Eluting Coronary Stent System (EECSS) | Other | Preclinical | Angioplasty | COMPLETED | NCT01249027 |
| XIENCE V® Everolimus Eluting Coronary Stent System (EECSS) | Other | Preclinical | Angioplasty | COMPLETED | NCT01249027 |
| ABT-888 | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| Temozolomide | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| ABT-888 | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| Temozolomide | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| ABT-888 | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| Temozolomide | Other | Phase PHASE2 | Colorectal Cancer | COMPLETED | NCT01051596 |
| Everolimus Eluting BVS | Other | Approved | Atherosclerosis | TERMINATED | NCT01341340 |
| Everolimus Eluting BVS | Other | Approved | Atherosclerosis | TERMINATED | NCT01341340 |
| Device closure with the AMPLATZER PFO Occluder | Device | Preclinical | Patent Foramen Ovale | APPROVED_FOR_MARKETING | NCT00584064 |
| CRT-D System | Other | Preclinical | Heart Failure | COMPLETED | NCT01555619 |
| Therapy Cool Path Duo Cardiac Ablation System | Drug | Approved | Ischemic Ventricular Tachycardia | TERMINATED | NCT00925522 |
| Therapy Cool Path Duo Cardiac Ablation System | Drug | Approved | Ischemic Ventricular Tachycardia | TERMINATED | NCT00925522 |
| Tube Feeding Product | Other | Preclinical | Malnutrition | COMPLETED | NCT03459001 |
| IBS | Other | Preclinical | Irritable Bowel Syndrome | COMPLETED | NCT03549143 |
| IBS | Other | Preclinical | Irritable Bowel Syndrome | COMPLETED | NCT03549143 |
| Axium DRG Neurostimulator | Other | Preclinical | Chronic Post Surgical Pain | TERMINATED | NCT02335229 |
| 2.25 mm XIENCE V® Everolimus Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | TERMINATED | NCT00783796 |
| IDev SUPERA® Interwoven Self Expanding Nitinol Stent Peripheral Vascular System | Other | Approved | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | WITHDRAWN | NCT00613418 |
| IDev SUPERA® Interwoven Self Expanding Nitinol Stent Peripheral Vascular System | Other | Approved | With de Novo or Restenotic Lesions in the Common and/or External Iliac Arteries | WITHDRAWN | NCT00613418 |
| coronary artery bypass graft surgery | Procedure | Approved | Coronary Artery Disease | TERMINATED | NCT00997828 |
| everolimus-eluting stent | Other | Approved | Coronary Artery Disease | TERMINATED | NCT00997828 |
| Conventional RF ablation | Other | Approved | Paroxysmal Atrial Fibrillation | TERMINATED | NCT02703454 |
| FIRM-guided RF ablation | Other | Approved | Paroxysmal Atrial Fibrillation | TERMINATED | NCT02703454 |
| Reprogramming of spinal cord stimulator (Proclaim or Prodigy SJM internal pulse generator) parameters according to study protocol | Other | Approved | Chronic Pain | COMPLETED | NCT02896361 |
| Mebeverine | Other | Preclinical | Post-cholecystectomy Gastrointestinal Spasms | COMPLETED | NCT02260154 |
| Mebeverine | Other | Preclinical | Post-cholecystectomy Gastrointestinal Spasms | COMPLETED | NCT02260154 |
| Mebeverine | Other | Preclinical | Post-cholecystectomy Gastrointestinal Spasms | COMPLETED | NCT02260154 |
| Mebeverine | Other | Preclinical | Post-cholecystectomy Gastrointestinal Spasms | COMPLETED | NCT02260154 |
| ACIST Navvus Microcatheter | Other | Approved | Ischemia | COMPLETED | NCT02648230 |
| St. Jude Medical Pressure Wire | Other | Approved | Ischemia | COMPLETED | NCT02648230 |
| Treatment with CSI atherectomy device | Drug | Approved | Peripheral Vascular Diseases | TERMINATED | NCT03455374 |
| Device closure with the AMPLATZER Muscular VSD Occluder | Device | Approved | Heart Septal Defects, Ventricular | COMPLETED | NCT00583791 |
| Device closure with the AMPLATZER Muscular VSD Occluder | Device | Approved | Heart Septal Defects, Ventricular | COMPLETED | NCT00583791 |
| mCPVA | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT02571218 |
| Substrate+mCPVA | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT02571218 |
| AMPLATZER Septal Occluder | Other | Approved | Atrial Septal Defect | COMPLETED | NCT00650936 |
| Placebo | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194116 |
| Divalproex Sodium ER | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194116 |
| Placebo | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194116 |
| Divalproex Sodium ER | Other | Phase PHASE3 | Bipolar Disorder | COMPLETED | NCT00194116 |
| SJM Implantable cardiac devices | Device | Preclinical | Bradycardia | COMPLETED | NCT03012568 |
| Radio-frequency Ablation | Other | Preclinical | Ventricular Outflow Tract Tachycardia | COMPLETED | NCT02722577 |
| Radio-frequency Ablation | Other | Preclinical | Ventricular Outflow Tract Tachycardia | COMPLETED | NCT02722577 |
| CRT Patients | Other | Preclinical | Heart Failure | COMPLETED | NCT01805154 |
| CRT Patients | Other | Preclinical | Heart Failure | COMPLETED | NCT01805154 |
| Implantation of a QuickFlex® μ Model 1258T LV Lead | Other | Preclinical | Heart Failure | COMPLETED | NCT01179477 |
| Guideline-directed medical therapy | Drug | Approved | Mitral Regurgitation | UNKNOWN | NCT03705312 |
| Transcatheter mitral valve repair | Other | Approved | Mitral Regurgitation | UNKNOWN | NCT03705312 |
| AF ablation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT03989726 |
| AF ablation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT03989726 |
| Placebo | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00807586 |
| Solumedrol | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00807586 |
| Placebo | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00807586 |
| Solumedrol | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00807586 |
| Non-Diagnostic Cardiac MRI scan | Other | Approved | Bradycardia | COMPLETED | NCT02041702 |
| Non-Diagnostic Cardiac MRI scan | Other | Approved | Bradycardia | COMPLETED | NCT02041702 |
| Pacemaker, ICD, or CRT device | Device | Approved | Cardiac Arrhythmia | COMPLETED | NCT02807948 |
| Metabolic Flexibility Tests | Other | Approved | Energy Metabolism | COMPLETED | NCT03701867 |
| Accelerometry | Other | Approved | Chronic Pain | COMPLETED | NCT02950831 |
| Receive Detailed ICD Information-paper | Other | Approved | Implantable Cardioverter-Defibrillator | COMPLETED | NCT02989090 |
| Receive Detailed ICD Information-electronic | Other | Approved | Implantable Cardioverter-Defibrillator | COMPLETED | NCT02989090 |
| quetiapine | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| divalproex ER | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| quetiapine | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| divalproex ER | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| quetiapine | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| divalproex ER | Other | Phase PHASE4 | Bipolar Disorder | COMPLETED | NCT00397020 |
| Observational | Other | Preclinical | Heart Failure, Unspecified | TERMINATED | NCT03001141 |
| Observational | Other | Preclinical | Heart Failure, Unspecified | TERMINATED | NCT03001141 |
| Standard of care | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01132495 |
| OMT | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01132495 |
| Stenting plus OMT | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01132495 |
| intravaginal progesterone gel 90 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT02491437 |
| Dydrogesterone 30 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT02491437 |
| intravaginal progesterone gel 90 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT02491437 |
| Dydrogesterone 30 mg | Other | Phase PHASE3 | Female Infertility | COMPLETED | NCT02491437 |
| Optimization using echocardiography | Other | Approved | Heart Failure | COMPLETED | NCT01172067 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT01172067 |
| Optimization using echocardiography | Other | Approved | Heart Failure | COMPLETED | NCT01172067 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT01172067 |
| Implantation with the commercially available Axium neurostimulator | Other | Preclinical | Peripheral Neuropathy | TERMINATED | NCT02349646 |
| EnligHTN™ Renal Denervation System | Other | Preclinical | Uncontrolled Hypertension | COMPLETED | NCT02006758 |
| ORS | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT03463512 |
| Racecadotril plus ORS | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT03463512 |
| ORS | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT03463512 |
| Racecadotril plus ORS | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT03463512 |
| MediGuide™ | Other | Approved | Heart Failure | COMPLETED | NCT01519739 |
| Abbott Vascular ABSORB Everolimus Eluting Bioresorbable Vascular Scaffold System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01425281 |
| Abbott Vascular XIENCE Everolimus Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01425281 |
| Absorb BVS System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01923740 |
| XIENCE V EECSS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01923740 |
| Absorb BVS System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01923740 |
| XIENCE V EECSS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01923740 |
| Transcatheter PDA Closure | Other | Preclinical | Ductus Arteriosus, Patent | NOT_YET_RECRUITING | NCT04205877 |
| Transcatheter PDA Closure | Other | Preclinical | Ductus Arteriosus, Patent | NOT_YET_RECRUITING | NCT04205877 |
| XIENCE PRIME - Core Size | Other | Preclinical | Angina | COMPLETED | NCT01721096 |
| XIENCE PRIME - Long Length (LL) | Other | Preclinical | Angina | COMPLETED | NCT01721096 |
| XIENCE PRIME - Core Size | Other | Preclinical | Angina | COMPLETED | NCT01721096 |
| XIENCE PRIME - Long Length (LL) | Other | Preclinical | Angina | COMPLETED | NCT01721096 |
| Group 2 Nutritional Shake | Other | Approved | Glycemic Control | COMPLETED | NCT04230889 |
| Group 1 Nutritional Shake | Other | Approved | Glycemic Control | COMPLETED | NCT04230889 |
| Usual Diet Group | Other | Approved | Glycemic Control | COMPLETED | NCT04230889 |
| toric intraocular lens | Other | Approved | Cataract | COMPLETED | NCT02566083 |
| non-toric intraocular lens | Other | Approved | Cataract | COMPLETED | NCT02566083 |
| Algorithmic Cardiac Resynchronisation Therapy Optimisation | Drug | Approved | Heart Failure, Systolic | WITHDRAWN | NCT02997670 |
| Algorithmic Cardiac Resynchronisation Therapy Optimisation | Drug | Approved | Heart Failure, Systolic | WITHDRAWN | NCT02997670 |
| Presbyopia and astigmatism correcting intraocular lens | Other | Approved | Cataract Bilateral | COMPLETED | NCT03082599 |
| Amiodarone | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Ablation | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Amiodarone | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Ablation | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Amiodarone | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Ablation | Other | Phase PHASE3 | Defibrillators, Implantable | TERMINATED | NCT01097330 |
| Flavonoid Cohort 3 | Other | Approved | Biological Aging | COMPLETED | NCT03213340 |
| Curcuminoid Cohort 2 | Other | Approved | Biological Aging | COMPLETED | NCT03213340 |
| Catechin Cohort 1 | Other | Approved | Biological Aging | COMPLETED | NCT03213340 |
| Experimental Hydrolyzed Protein Infant Formula | Other | Approved | Protein Intolerance | COMPLETED | NCT03884309 |
| Fractional Flow Reserve | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02935088 |
| Fractional Flow Reserve | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02935088 |
| Firm ablation for transitional AF rotors | Other | Approved | Atrial Fibrillation | WITHDRAWN | NCT02758002 |
| Firm ablation for transitional AF rotors | Other | Approved | Atrial Fibrillation | WITHDRAWN | NCT02758002 |
| Compliance | Other | Preclinical | Epilepsy | COMPLETED | NCT00356018 |
| Compliance | Other | Preclinical | Epilepsy | COMPLETED | NCT00356018 |
| Patients implanted with a St. Jude Medical pacemakers | Other | Preclinical | Standard Bradycardia Pacing Indication | COMPLETED | NCT02577887 |
| Abbott, Inc Confirm Rx™ versus Medtronic, Inc Reveal LINQTM | Other | Approved | Cardiac Arrythmias | COMPLETED | NCT03720639 |
| Abbott, Inc Confirm Rx™ versus Medtronic, Inc Reveal LINQTM | Other | Approved | Cardiac Arrythmias | COMPLETED | NCT03720639 |
| Stimulation will be delivered at with different microdosing setting to identify the optimal parameter values for each patient. | Other | Approved | Pain, Intractable | COMPLETED | NCT03350256 |
| Glucose tablets | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| Azithromycin 500Mg Oral Tablet | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| Hydroxychloroquine 200 Mg Oral Tablet | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| Glucose tablets | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| Azithromycin 500Mg Oral Tablet | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| Hydroxychloroquine 200 Mg Oral Tablet | Other | Phase PHASE3 | COVID19 | UNKNOWN | NCT04328272 |
| CABG | Other | Approved | Chronic Coronary Occlusion | COMPLETED | NCT01205776 |
| Percutaneous Coronary Intervention | Other | Approved | Chronic Coronary Occlusion | COMPLETED | NCT01205776 |
| AMPLATZER Cardiac Plug | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01118299 |
| Left atrial appendage closure | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT04180605 |
| Additional support for preoperative planning of LAA closure procedures | Procedure | Approved | Atrial Fibrillation | UNKNOWN | NCT04180605 |
| Left atrial appendage closure | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT04180605 |
| Additional support for preoperative planning of LAA closure procedures | Procedure | Approved | Atrial Fibrillation | UNKNOWN | NCT04180605 |
| Experimental Product | Other | Approved | Compliance, Patient | TERMINATED | NCT04041908 |
| Cardiac Ablation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01907828 |
| Renal Artery Ablation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT01907828 |
| XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) | Other | Preclinical | Angioplasty | COMPLETED | NCT01894152 |
| Iliac segment recanalization, stenting and plastic Common Femoral Artery (CFA) patch | Other | Approved | Atherosclerosis of the Peripheral Arteries | UNKNOWN | NCT03315884 |
| Iliac segment recanalization and stenting Iliac segment Common Femoral Artery (CFA) | Other | Approved | Atherosclerosis of the Peripheral Arteries | UNKNOWN | NCT03315884 |
| Endovascular treatment for PAD | Drug | Approved | Atherosclerosis | UNKNOWN | NCT03951727 |
| Endovascular treatment for PAD | Drug | Approved | Atherosclerosis | UNKNOWN | NCT03951727 |
| Multidisciplinary Team Based Care Model | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT04427124 |
| Multidisciplinary Team Based Care Model | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT04427124 |
| Multidisciplinary Team Based Care Model | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT04427124 |
| Navigation | Other | Preclinical | Peripheral Arterial Disease | COMPLETED | NCT03585387 |
| Different formulations of once-daily lopinavir/ritonavir | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00281606 |
| Different formulations of once-daily lopinavir/ritonavir | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00281606 |
| Different formulations of once-daily lopinavir/ritonavir | Other | Phase PHASE4 | HIV Infection | COMPLETED | NCT00281606 |
| OCT stent guidance | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT01663896 |
| Cardiac MRI with and without pacemaker stimulation | Other | Approved | Heart Block | TERMINATED | NCT01798043 |
| Cardiac MRI with pacemaker stimulation | Other | Approved | Heart Block | TERMINATED | NCT01798043 |
| AMPLATZER PFO Occluder | Other | Approved | Migraine Headaches | COMPLETED | NCT00355056 |
| Sham Procedure | Procedure | Approved | Migraine Headaches | COMPLETED | NCT00355056 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03781258 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03781258 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03781258 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03704220 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03704220 |
| Warfarin | Other | Approved | Heart Failure | UNKNOWN | NCT03078374 |
| Drug (Direct thrombin or Factor Xa inhibitor) | Drug | Approved | Atrial Fibrillation | TERMINATED | NCT01650298 |
| Drug (Direct thrombin or Factor Xa inhibitor) | Drug | Approved | Atrial Fibrillation | TERMINATED | NCT01650298 |
| Placebo | Other | Preclinical | CKD Stage 3/4 | COMPLETED | NCT02018133 |
| Vitamin D 2mg daily for 2 weeks oral paricalcitol | Other | Preclinical | CKD Stage 3/4 | COMPLETED | NCT02018133 |
| Placebo | Other | Preclinical | CKD Stage 3/4 | COMPLETED | NCT02018133 |
| Vitamin D 2mg daily for 2 weeks oral paricalcitol | Other | Preclinical | CKD Stage 3/4 | COMPLETED | NCT02018133 |
| Adalimumab | Other | Phase PHASE2 | Sarcoidosis | TERMINATED | NCT00311246 |
| Adalimumab | Other | Phase PHASE2 | Sarcoidosis | TERMINATED | NCT00311246 |
| Ellipse VR ICD and Durata/Optisure lead | Other | Approved | Implantable Defibrillator User | COMPLETED | NCT02787291 |
| Ellipse VR ICD and Durata/Optisure lead | Other | Approved | Implantable Defibrillator User | COMPLETED | NCT02787291 |
| Reference Group | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Experimental Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Control Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Reference Group | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Experimental Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Control Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT03967132 |
| Nutritional Supplement | Other | Approved | Glycemic Response | COMPLETED | NCT04313920 |
| Nutritional Supplement | Other | Approved | Glycemic Response | COMPLETED | NCT04313920 |
| Device data collection | Device | Preclinical | Sick Sinus Syndrome | COMPLETED | NCT03564860 |
| Absorb™ BVS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01844284 |
| XIENCE PRIME®/XIENCE Xpedition™ | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01844284 |
| Omacor (Omega-3-acid ethyl esters) | Other | Preclinical | History of Myocardial Infarction | COMPLETED | NCT03415152 |
| Omacor (Omega-3-acid ethyl esters) | Other | Preclinical | History of Myocardial Infarction | COMPLETED | NCT03415152 |
| Omacor (Omega-3-acid ethyl esters) | Other | Preclinical | History of Myocardial Infarction | COMPLETED | NCT03415152 |
| HeartPOD™ System | Other | Preclinical | Heart Failure | COMPLETED | NCT00632372 |
| Cardiac Resynchronization Therapy | Drug | Preclinical | Heart Failure | COMPLETED | NCT00632372 |
| HeartPOD™ System | Other | Preclinical | Heart Failure | COMPLETED | NCT00632372 |
| Cardiac Resynchronization Therapy | Drug | Preclinical | Heart Failure | COMPLETED | NCT00632372 |
| Angiography-only | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04597489 |
| Fractional flow reserve | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04597489 |
| Angiography-only | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04597489 |
| Fractional flow reserve | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04597489 |
| Placebo | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| adalimumab | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| Placebo | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| adalimumab | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| Placebo | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| adalimumab | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| Placebo | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| adalimumab | Other | Approved | Arthritis, Rheumatoid | COMPLETED | NCT01197144 |
| Mindfulness Meditation | Other | Approved | Hand Injuries | COMPLETED | NCT03458013 |
| Accent MRI system (with MRI scan) | Other | Approved | Adverse Effect of MRI on an Implanted Pacemaker Lead | COMPLETED | NCT01576016 |
| Accent MRI system (lead safety) | Other | Approved | Adverse Effect of MRI on an Implanted Pacemaker Lead | COMPLETED | NCT01576016 |
| Rosuvastatin | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00184951 |
| FreeStyle Libre 3 | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT04464772 |
| CRT | Other | Preclinical | Chronic Heart Failure | COMPLETED | NCT02367716 |
| CRT | Other | Preclinical | Chronic Heart Failure | COMPLETED | NCT02367716 |
| Once daily | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT00679926 |
| Once daily | Other | Phase PHASE4 | HIV Infections | TERMINATED | NCT00679926 |
| Placebo Micronized progesterone | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Placebo Dydrogesterone oral tablet | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Micronized progesterone | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Dydrogesterone Oral Tablet | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Placebo Micronized progesterone | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Placebo Dydrogesterone oral tablet | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Micronized progesterone | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| Dydrogesterone Oral Tablet | Other | Phase PHASE4 | Infertility, Female | COMPLETED | NCT03677336 |
| CRT-P Implant | Other | Approved | Hypertrophic Cardiomyopathy With Obstruction | COMPLETED | NCT01614717 |
| CRT-P Implant | Other | Approved | Hypertrophic Cardiomyopathy With Obstruction | COMPLETED | NCT01614717 |
| Optical coherence tomography assessment | Other | Approved | Tomography, Optical Coherence | UNKNOWN | NCT04683133 |
| Optical coherence tomography assessment | Other | Approved | Tomography, Optical Coherence | UNKNOWN | NCT04683133 |
| Optical coherence tomography assessment | Other | Approved | Tomography, Optical Coherence | UNKNOWN | NCT04683133 |
| lead placement followed by BurstDR stimulation | Other | Approved | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | COMPLETED | NCT03277378 |
| lead placement followed by BurstDR stimulation | Other | Approved | Chronic, Intractable Pain of the Trunk and/or Lower Limbs | COMPLETED | NCT03277378 |
| Experimental Infant Formula | Other | Approved | Growth and Tolerance | COMPLETED | NCT04105686 |
| Control Infant Formula | Other | Approved | Growth and Tolerance | COMPLETED | NCT04105686 |
| RV Pacing | Other | Approved | Atrioventricular Block | COMPLETED | NCT00187278 |
| Biventricular Pacing | Other | Approved | Atrioventricular Block | COMPLETED | NCT00187278 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | TERMINATED | NCT03448367 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | TERMINATED | NCT03448367 |
| BiV/MPP | Other | Preclinical | Heart Failure | COMPLETED | NCT02832622 |
| MPP | Other | Preclinical | Heart Failure | COMPLETED | NCT02832622 |
| DAPT | Other | Approved | Bleeding Disorder | COMPLETED | NCT03355742 |
| XIENCE | Other | Approved | Bleeding Disorder | COMPLETED | NCT03355742 |
| Low-intensity exercise therapy | Drug | Approved | Pancreatic Cancer | TERMINATED | NCT03244683 |
| Nutrition counseling | Other | Approved | Pancreatic Cancer | TERMINATED | NCT03244683 |
| Ensure Surgical | Other | Approved | Pancreatic Cancer | TERMINATED | NCT03244683 |
| Omega-3-acid ethyl ester or Placebo | Other | Phase PHASE3 | Hypertriglyceridemia | COMPLETED | NCT04756180 |
| Omega-3-acid ethyl ester or Placebo | Other | Phase PHASE3 | Hypertriglyceridemia | COMPLETED | NCT04756180 |
| Oral Nutritional Supplement | Other | Approved | Malnutrition | COMPLETED | NCT03245047 |
| Oral Nutritional Supplement with AN 777 | Other | Approved | Malnutrition | COMPLETED | NCT03245047 |
| Coronary artery stenting: Absorb BVS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02229864 |
| preset program | Other | Approved | Chronic Pain | COMPLETED | NCT02346383 |
| Experimental Thickener | Other | Approved | Gastro-intestinal Tolerance | WITHDRAWN | NCT04104815 |
| Coronary PCI guided by Angiography | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02471586 |
| Coronary PCI guided by OCT | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02471586 |
| Coronary PCI guided by IVUS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02471586 |
| 10 Hz rTMS | Other | Approved | Schizophrenia | TERMINATED | NCT02242578 |
| 1 Hz rTMS | Other | Approved | Schizophrenia | TERMINATED | NCT02242578 |
| blood taking | Other | Preclinical | Chest Pain | COMPLETED | NCT02789904 |
| Possible NSTE-ACS | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT04851418 |
| Possible NSTE-ACS | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT04851418 |
| Rate or Rhythm Control Therapy | Drug | Approved | Atrial Fibrillation | COMPLETED | NCT00911508 |
| Left atrial ablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT00911508 |
| Glucerna | Other | Phase PHASE3 | Hypoglycemia | UNKNOWN | NCT03802942 |
| Glucerna | Other | Phase PHASE3 | Hypoglycemia | UNKNOWN | NCT03802942 |
| Blood drawing to determine drug levels | Drug | Preclinical | HIV Infections | COMPLETED | NCT00179335 |
| Blood drawing to determine drug levels | Drug | Preclinical | HIV Infections | COMPLETED | NCT00179335 |
| Anatomical midline lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| Paresthesia mapping lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| Anatomical midline lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| Paresthesia mapping lead evaluation first | Other | Approved | Chronic Pain | COMPLETED | NCT02986074 |
| Cardiac Rhythm Management device | Device | Preclinical | Bradycardia | COMPLETED | NCT01754064 |
| XIENCE Xpedition 2.25 mm stent | Other | Preclinical | Ischemic Heart Disease | COMPLETED | NCT02513732 |
| Toddler Drink for HM group | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Supplemental Formula for HM Group | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Experimental Toddler Drink | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Experimental Infant Formula | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Control Toddler Drink | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Control Infant Formula | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Toddler Drink for HM group | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Supplemental Formula for HM Group | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Experimental Toddler Drink | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Experimental Infant Formula | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Control Toddler Drink | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| Control Infant Formula | Other | Approved | Respiratory Infections in Children | TERMINATED | NCT04495738 |
| EnligHTN | Other | Preclinical | Hypertension | TERMINATED | NCT01705080 |
| DBS | Other | Preclinical | Parkinson | COMPLETED | NCT03630302 |
| Osmolite | Other | Approved | Enteral Nutrition | COMPLETED | NCT03153397 |
| Nutraflora scFOS | Other | Approved | Enteral Nutrition | COMPLETED | NCT03153397 |
| Osmolite | Other | Approved | Enteral Nutrition | COMPLETED | NCT03153397 |
| Nutraflora scFOS | Other | Approved | Enteral Nutrition | COMPLETED | NCT03153397 |
| MRI scan | Other | Approved | Chronic Pain | COMPLETED | NCT02738840 |
| MRI scan | Other | Approved | Chronic Pain | COMPLETED | NCT02738840 |
| High Protein, Energy Dense Nutritional Supplement | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT04259437 |
| High Protein, Energy Dense Nutritional Supplement | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT04259437 |
| AVJ-514 | Other | Approved | Mitral Stenosis With Insufficiency | COMPLETED | NCT02520310 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03448380 |
| FreeStyle Libre Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT03448380 |
| Adalimumab | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT01716039 |
| MTX 25 | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT01716039 |
| MTX 12.5 | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT01716039 |
| Device interrogation | Device | Preclinical | Heart Failure | UNKNOWN | NCT04397224 |
| Device interrogation | Device | Preclinical | Heart Failure | UNKNOWN | NCT04397224 |
| Prodigy, Prodigy MRI or Proclaim Elite IPG | Other | Approved | Chronic Pain | COMPLETED | NCT03082261 |
| Experimental Infant Formula | Other | Approved | Tolerance | COMPLETED | NCT04529759 |
| Control Infant Formula | Other | Approved | Tolerance | COMPLETED | NCT04529759 |
| Standard Care | Other | Approved | Palliative Care | UNKNOWN | NCT04942756 |
| Continuous Glucose Monitoring | Other | Approved | Palliative Care | UNKNOWN | NCT04942756 |
| Standard Care | Other | Approved | Palliative Care | UNKNOWN | NCT04942756 |
| Continuous Glucose Monitoring | Other | Approved | Palliative Care | UNKNOWN | NCT04942756 |
| Amiodarone | Other | Phase PHASE3 | Heart Diseases | COMPLETED | NCT02924285 |
| Procedure (Radiofrequency catheter ablation) | Procedure | Phase PHASE3 | Heart Diseases | COMPLETED | NCT02924285 |
| Medication stabilized the condition | Drug | Approved | ST Elevation Myocardial Infarction | UNKNOWN | NCT04996277 |
| Fibrinolytic therapy | Drug | Approved | ST Elevation Myocardial Infarction | UNKNOWN | NCT04996277 |
| Thrombus suction | Other | Approved | ST Elevation Myocardial Infarction | UNKNOWN | NCT04996277 |
| angiography | Other | Approved | ST Elevation Myocardial Infarction | UNKNOWN | NCT04996277 |
| Intervention/treatment | Drug | Approved | Bradycardia | COMPLETED | NCT00311168 |
| Intervention/treatment | Drug | Approved | Bradycardia | COMPLETED | NCT00311168 |
| amiodarone hydrochloride | Other | Approved | Chagas Cardiomyopathy | UNKNOWN | NCT01722942 |
| ICD implantation | Other | Approved | Chagas Cardiomyopathy | UNKNOWN | NCT01722942 |
| HeartPOD™ System | Other | Approved | Heart Failure | COMPLETED | NCT00547729 |
| Nurse led structured intervention - hypoglycaemia education and diabetes treatment modification modification | Drug | Approved | Type 2 Diabetes | UNKNOWN | NCT04997512 |
| Freestyle libre | Other | Approved | Type 2 Diabetes | UNKNOWN | NCT04997512 |
| Endovascular treatment for PAD during medical care (SuperA stent (Abbott)) | Drug | Preclinical | Atherosclerosis Obliterans | COMPLETED | NCT03020290 |
| Control Infant Formula | Other | Approved | Infant Development | COMPLETED | NCT04006236 |
| Experimental Infant Formula | Other | Approved | Infant Development | COMPLETED | NCT04006236 |
| Directional Deep Brain Stimulation of STN | Other | Approved | Parkinson Disease | UNKNOWN | NCT03548506 |
| Omnidirectional Deep Brain Stimulation of STN | Other | Approved | Parkinson Disease | UNKNOWN | NCT03548506 |
| TactiCath Quartz treatment | Drug | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT02310100 |
| Observational study | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01476956 |
| Observational study | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01476956 |
| Zidovudine | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| Anti-HIV Immune Serum Globulin (Human) | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| Zidovudine | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| Anti-HIV Immune Serum Globulin (Human) | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| Zidovudine | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| Anti-HIV Immune Serum Globulin (Human) | Other | Phase PHASE2 | HIV Infections | TERMINATED | NCT00000961 |
| DAPT | Other | Approved | Coronary Artery Lesions | COMPLETED | NCT03218787 |
| XIENCE | Other | Approved | Coronary Artery Lesions | COMPLETED | NCT03218787 |
| Fractional Flow Reserve (FFR) | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Angiography guided PCI | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Fractional Flow Reserve (FFR) | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Angiography guided PCI | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Fractional Flow Reserve (FFR) | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Angiography guided PCI | Other | Approved | Acute ST Segment Elevation Myocardial Infarction | UNKNOWN | NCT02943954 |
| Portico Valve and FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | COMPLETED | NCT03724812 |
| Creon® 10000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Creon® 25000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Creon® 10000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Creon® 25000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Creon® 10000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Creon® 25000 | Other | Phase PHASE3 | Pancreatic Insufficiency | UNKNOWN | NCT03450772 |
| Tricor (fenofibrate), 145 mg, film-coated tablet | Other | Preclinical | Hypertriglyceridemia | COMPLETED | NCT04650152 |
| LASIK correction of hyperopic refractive errors | Other | Approved | Hyperopia | COMPLETED | NCT01675479 |
| LASIK correction of hyperopic refractive errors | Other | Approved | Hyperopia | COMPLETED | NCT01675479 |
| Duphaston® (Dydrogesteron) | Other | Preclinical | Infertility | UNKNOWN | NCT04249297 |
| Duphaston® (Dydrogesteron) | Other | Preclinical | Infertility | UNKNOWN | NCT04249297 |
| Duphaston® (Dydrogesteron) | Other | Preclinical | Infertility | UNKNOWN | NCT04249297 |
| Duphaston® (Dydrogesterone) | Other | Preclinical | Endometriosis | COMPLETED | NCT03690765 |
| Duphaston® (Dydrogesterone) | Other | Preclinical | Endometriosis | COMPLETED | NCT03690765 |
| Experimental Nutritional Pudding | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT04945083 |
| Experimental Nutritional Pudding | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT04945083 |
| Manual Compression | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| Percutaneous Closure | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| Manual Compression | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| Percutaneous Closure | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| Manual Compression | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| Percutaneous Closure | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04180540 |
| MitraClip NTR/XTR System | Other | Preclinical | Mitral Valve Regurgitation | COMPLETED | NCT03502811 |
| MitraClip NTR/XTR System | Other | Preclinical | Mitral Valve Regurgitation | COMPLETED | NCT03502811 |
| Esophageal high-resolution manometry and 24-h esophageal pH-impedance monitoring | Other | Approved | Gastroesophageal Reflux Disease (GERD) | COMPLETED | NCT02699060 |
| Upper gastrointestinal endoscopy with biopsy and collection of refluxate | Other | Approved | Gastroesophageal Reflux Disease (GERD) | COMPLETED | NCT02699060 |
| Esophageal high-resolution manometry and 24-h esophageal pH-impedance monitoring | Other | Approved | Gastroesophageal Reflux Disease (GERD) | COMPLETED | NCT02699060 |
| Upper gastrointestinal endoscopy with biopsy and collection of refluxate | Other | Approved | Gastroesophageal Reflux Disease (GERD) | COMPLETED | NCT02699060 |
| MPP ON | Other | Approved | Heart Failure | COMPLETED | NCT02476201 |
| Clinical Management Recommendations for reducing pump thrombosis | Other | Approved | HeartMate II Pump Thrombosis | COMPLETED | NCT02158403 |
| Drug: Avelox® 400Mg Tablet | Drug | Phase PHASE1 | Bioequivalence | COMPLETED | NCT05307614 |
| Moksi® 400mg Tablet | Other | Phase PHASE1 | Bioequivalence | COMPLETED | NCT05307614 |
| ABSORB Scaffold | Other | Preclinical | Coronary Artery Stenosis | COMPLETED | NCT02066623 |
| CardioMEMS HF System | Other | Approved | Heart Failure | COMPLETED | NCT02693691 |
| CardioMEMS HF System | Other | Approved | Heart Failure | COMPLETED | NCT02693691 |
| Comprehensive functional diagnostics of coronary circulation | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT05313919 |
| Comprehensive functional diagnostics of coronary circulation | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT05313919 |
| LV pacing site | Other | Approved | Arrythmia | COMPLETED | NCT02057588 |
| LV pacing site | Other | Approved | Arrythmia | COMPLETED | NCT02057588 |
| 3T MRI scan | Other | Preclinical | Syncope | COMPLETED | NCT03786640 |
| Intravenous Bolus Furosemide | Other | Approved | Heart Failure | COMPLETED | NCT04235062 |
| Ringer's (8.6 g/L sodium chloride, 0.33 g/L calcium chloride, 0.3 g/L potassium chloride) Solution | Other | Approved | Heart Failure | COMPLETED | NCT04235062 |
| Intravenous Bolus Furosemide | Other | Approved | Heart Failure | COMPLETED | NCT04235062 |
| Ringer's (8.6 g/L sodium chloride, 0.33 g/L calcium chloride, 0.3 g/L potassium chloride) Solution | Other | Approved | Heart Failure | COMPLETED | NCT04235062 |
| Amino Acid-Based Experimental Study Formula | Other | Approved | Food Allergy | TERMINATED | NCT04127656 |
| TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™ | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03650556 |
| DAPT (aspirin and/or P2Y12 receptor inhibitor) | Other | Approved | Bleeding Disorder | COMPLETED | NCT03815175 |
| XIENCE | Other | Approved | Bleeding Disorder | COMPLETED | NCT03815175 |
| Tranexamic acid injection | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05362500 |
| Glycolic Acid 70% | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05362500 |
| Tranexamic acid injection | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05362500 |
| Glycolic Acid 70% | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05362500 |
| ILR implantation | Other | Preclinical | Heart Failure With Preserved Ejection Fraction (HFpEF) | COMPLETED | NCT01989299 |
| Midazolam | Other | Preclinical | Delirium | COMPLETED | NCT00417664 |
| Propofol | Other | Preclinical | Delirium | COMPLETED | NCT00417664 |
| Dexmedetomidine | Other | Preclinical | Delirium | COMPLETED | NCT00417664 |
| PEVAR (Prostar XL closure) | Other | Approved | Abdominal Aortic Aneurysm | COMPLETED | NCT01070069 |
| SEVAR (IntuiTrak) | Other | Approved | Abdominal Aortic Aneurysm | COMPLETED | NCT01070069 |
| PEVAR (ProGlide closure) | Other | Approved | Abdominal Aortic Aneurysm | COMPLETED | NCT01070069 |
| Prone Positioning Maneuver | Other | Approved | COVID-19 Acute Respiratory Distress Syndrome | COMPLETED | NCT05405335 |
| Prone Positioning Maneuver | Other | Approved | COVID-19 Acute Respiratory Distress Syndrome | COMPLETED | NCT05405335 |
| Study Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | TERMINATED | NCT04934397 |
| MitraClip Procedure | Procedure | Approved | Functional Mitral Regurgitation | COMPLETED | NCT04350372 |
| Current Regimen | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00145795 |
| Kaletra + Current Dual NRTI Backbone | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00145795 |
| Current Regimen | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00145795 |
| Kaletra + Current Dual NRTI Backbone | Other | Phase PHASE4 | HIV Infections | COMPLETED | NCT00145795 |
| AMPLATZER™ Cardiac Plug | Other | Preclinical | Non-valvular Atrial Fibrillation (NVAF) | COMPLETED | NCT02954237 |
| HeartMate 3™ | Other | Approved | Heart Failure | COMPLETED | NCT02475460 |
| Less Invasive Surgery (LIS) | Procedure | Approved | Heart Failure | COMPLETED | NCT02475460 |
| Percutaneous Lead Management Kit | Other | Preclinical | Left Ventricular Assist Device | COMPLETED | NCT01485666 |
| Percutaneous Lead Management Kit | Other | Preclinical | Left Ventricular Assist Device | COMPLETED | NCT01485666 |
| CentriMag Ventricular Assist System | Other | Approved | Heart Failure | WITHDRAWN | NCT01171950 |
| HeartMate 3 LVAS | Other | Approved | Advanced Refractory Left Ventricular Heart Failure | COMPLETED | NCT02892955 |
| acetylsalicylic acid (ASA) therapy | Drug | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| Warfarin | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| HeartMate II (HMII) | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| acetylsalicylic acid (ASA) therapy | Drug | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| Warfarin | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| HeartMate II (HMII) | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT02836652 |
| HeartMate II LVAS | Other | Approved | Advanced Refractory Left Ventricular Heart Failure | COMPLETED | NCT02224755 |
| HeartMate 3 LVAS | Other | Approved | Advanced Refractory Left Ventricular Heart Failure | COMPLETED | NCT02224755 |
| CentriMag Ventricular Assist System | Other | Approved | Heart Failure | COMPLETED | NCT00819793 |
| CentriMag Ventricular Assist System | Other | Approved | Heart Failure | COMPLETED | NCT00819793 |
| Left Ventricular Assist System (LVAS) | Other | Approved | Heart Failure, Congestive | COMPLETED | NCT00121485 |
| Thoratec HeartMate II Left Ventricular Assist System (LVAS) | Other | Approved | Heart Failure, Congestive | COMPLETED | NCT00121472 |
| Thoratec HeartMate II Left Ventricular Assist System (LVAS) | Other | Approved | Heart Failure, Congestive | COMPLETED | NCT00121472 |
| Any Abiomed Impella® device approved for use in high-risk PCI | Device | Approved | Coronary Artery Disease | TERMINATED | NCT02468778 |
| HeartMate PHP | Other | Approved | Coronary Artery Disease | TERMINATED | NCT02468778 |
| Standard PPCI | Other | Approved | Acute Myocardial Infarction | UNKNOWN | NCT03447834 |
| Selective intracoronary hypothermia + PPCI | Other | Approved | Acute Myocardial Infarction | UNKNOWN | NCT03447834 |
| Blood test for Thyroid stimulating hormone (TSH) | Other | Preclinical | Hypothyroidism | UNKNOWN | NCT04784208 |
| Blood test for Thyroid stimulating hormone (TSH) | Other | Preclinical | Hypothyroidism | UNKNOWN | NCT04784208 |
| Test Meal | Other | Approved | Glycemic Control | COMPLETED | NCT05165693 |
| Experimental Formula | Other | Approved | Glycemic Control | COMPLETED | NCT05165693 |
| Test Meal | Other | Approved | Glycemic Control | COMPLETED | NCT05154045 |
| Experimental Formula | Other | Approved | Glycemic Control | COMPLETED | NCT05154045 |
| Self-Measurement Blood Glucose | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02776007 |
| Libre Flash CGMS | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02776007 |
| Self-Measurement Blood Glucose | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02776007 |
| Libre Flash CGMS | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02776007 |
| SMBG | Other | Preclinical | Diabetes Mellitus | TERMINATED | NCT04577976 |
| SMBG | Other | Preclinical | Diabetes Mellitus | TERMINATED | NCT04577976 |
| Budesonide | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Cortiment | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Budesonide | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Cortiment | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Budesonide | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Cortiment | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT05519514 |
| Aspirin 100 mg OD plus clopidogrel 75 mg OD | Other | Phase PHASE3 | Left Atrial Appendage Occlusion | UNKNOWN | NCT05554822 |
| Aspirin 100mg | Other | Phase PHASE3 | Left Atrial Appendage Occlusion | UNKNOWN | NCT05554822 |
| Randomization of Pre-knowledge of CT coronary venography | Other | Preclinical | Heart Failure - NYHA II - IV | COMPLETED | NCT01097733 |
| Randomization of Pre-knowledge of CT coronary venography | Other | Preclinical | Heart Failure - NYHA II - IV | COMPLETED | NCT01097733 |
| Itraconazole | Other | Phase PHASE1 | Onychomychosis | COMPLETED | NCT05567484 |
| Itraconazole | Other | Phase PHASE1 | Onychomychosis | COMPLETED | NCT05567484 |
| Removal of defibrillation coils and pulse generator | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT04809701 |
| Defibrillation following induction of VA (Configuration B first) | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT04809701 |
| Defibrillation following induction of VA (Configuration A first) | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT04809701 |
| Temporary implantation of defibrillation coils and pulse generator | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT04809701 |
| 0.03% tacrolimus twice daily was applied on group A patients with uvb phototherapy thrice daily | Drug | Phase PHASE1 | Vitiligo | COMPLETED | NCT05577637 |
| 0.03% tacrolimus twice daily was applied on group A patients with uvb phototherapy thrice daily | Drug | Phase PHASE1 | Vitiligo | COMPLETED | NCT05577637 |
| terbinafine | Other | Phase PHASE1 | Onychomycosis | COMPLETED | NCT05578950 |
| itraconazole | Other | Phase PHASE1 | Onychomycosis | COMPLETED | NCT05578950 |
| terbinafine | Other | Phase PHASE1 | Onychomycosis | COMPLETED | NCT05578950 |
| itraconazole | Other | Phase PHASE1 | Onychomycosis | COMPLETED | NCT05578950 |
| Cardiac resynchronization therapy by CRT-P or CRT-D implantation | Drug | Approved | Cardiac Resynchronization Therapy | COMPLETED | NCT04595305 |
| Mitomycin C | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Trabeculectomy | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Tube shunt surgery | Procedure | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Mitomycin C | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Trabeculectomy | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Tube shunt surgery | Procedure | Phase PHASE4 | Glaucoma | COMPLETED | NCT00666237 |
| Cryotherapy plus Salicylic Acid | Drug | Phase PHASE1 | Plantar Wart | COMPLETED | NCT05588999 |
| Cryotherapy Alone | Drug | Phase PHASE1 | Plantar Wart | COMPLETED | NCT05588999 |
| Cryotherapy plus Salicylic Acid | Drug | Phase PHASE1 | Plantar Wart | COMPLETED | NCT05588999 |
| Cryotherapy Alone | Drug | Phase PHASE1 | Plantar Wart | COMPLETED | NCT05588999 |
| Treatment with the Medtronic SCS System | Drug | Approved | Chronic Pain | TERMINATED | NCT02250469 |
| Treatment with the Axium SCS system | Drug | Approved | Chronic Pain | TERMINATED | NCT02250469 |
| angioplasty | Other | Approved | Coronary Artery Calcification | UNKNOWN | NCT05301218 |
| angioplasty | Other | Approved | Coronary Artery Calcification | UNKNOWN | NCT05301218 |
| potassium hydroxide | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05634460 |
| potassium hydroxide | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05634460 |
| Experimental Infant Formula | Other | Approved | Infant Development | COMPLETED | NCT03991949 |
| Experimental Infant Formula | Other | Approved | Infant Development | COMPLETED | NCT03991949 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | ACTIVE_NOT_RECRUITING | NCT04559945 |
| Aveir VR Leadless Pacemaker System | Other | Approved | Cardiac Rhythm Disorder | ACTIVE_NOT_RECRUITING | NCT04559945 |
| Study Infant Formula | Other | Approved | Gastro-Intestinal Tolerance | COMPLETED | NCT04915937 |
| Adalimumab and Infliximab | Other | Preclinical | Crohn's Disease | COMPLETED | NCT01338740 |
| HeartMate 3 Left Ventricular Assist System (HM3 LVAS) | Other | Preclinical | Advanced Refractory Left Ventricular Heart Failure | COMPLETED | NCT04548128 |
| Control | Other | Approved | Aging | WITHDRAWN | NCT02806765 |
| (1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methylheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol | Other | Approved | Aging | WITHDRAWN | NCT02806765 |
| 30% salicylic acid | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| 25% TRICHLOROACETIC ACID | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| 30% salicylic acid | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| 25% TRICHLOROACETIC ACID | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| 30% salicylic acid | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| 25% TRICHLOROACETIC ACID | Other | Approved | Acne Vulgaris | COMPLETED | NCT05712837 |
| Tricholoracetic acid | Other | Approved | Warts | COMPLETED | NCT05712811 |
| CRYOTHERAPY | Drug | Approved | Warts | COMPLETED | NCT05712811 |
| Standard Of Care | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04345497 |
| Diabetes-Specific Formula | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04345497 |
| Smart Coach | Other | Preclinical | Dyslipidemia | COMPLETED | NCT05370703 |
| My A:care | Other | Preclinical | Dyslipidemia | COMPLETED | NCT05370703 |
| CardioMems HF System | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05731466 |
| Prebiotic supplement | Other | Approved | Microbiome | COMPLETED | NCT03690999 |
| Placebo | Other | Approved | Microbiome | COMPLETED | NCT03690999 |
| Prebiotic supplement | Other | Approved | Microbiome | COMPLETED | NCT03690999 |
| Placebo | Other | Approved | Microbiome | COMPLETED | NCT03690999 |
| intralesional vitamin D3 | Other | Phase PHASE1 | Cutaneous Warts | COMPLETED | NCT05739786 |
| liq nitrogen | Other | Phase PHASE1 | Cutaneous Warts | COMPLETED | NCT05739786 |
| intralesional vitamin D3 | Other | Phase PHASE1 | Cutaneous Warts | COMPLETED | NCT05739786 |
| liq nitrogen | Other | Phase PHASE1 | Cutaneous Warts | COMPLETED | NCT05739786 |
| Control Group | Other | Approved | Undernutrition | COMPLETED | NCT05239208 |
| Oral Nutrition Supplement (ONS) Group | Other | Approved | Undernutrition | COMPLETED | NCT05239208 |
| Oral Nutritional Supplement (ONS) | Other | Approved | Malnutrition, Child | WITHDRAWN | NCT05437068 |
| COMPARISON OF THERAPEUTIC EFFICACY BETWEEN INTRALESIONAL BLEOMYCIN AND CRYOTHERAPY IN PLANTAR WARTS | Drug | Approved | Viral Wart | COMPLETED | NCT05752435 |
| COMPARISON OF THERAPEUTIC EFFICACY BETWEEN INTRALESIONAL BLEOMYCIN AND CRYOTHERAPY IN PLANTAR WARTS | Drug | Approved | Viral Wart | COMPLETED | NCT05752435 |
| Per cutaneous coronary intervention | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Coronary Angiography | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Optical Coherence Tomography | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Per cutaneous coronary intervention | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Coronary Angiography | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Optical Coherence Tomography | Other | Preclinical | Out of Hospital Cardiac Arrest | TERMINATED | NCT04431661 |
| Nutritional Intervention | Other | Approved | Bladder Cancer | RECRUITING | NCT05715684 |
| Exercise Training | Other | Approved | Bladder Cancer | RECRUITING | NCT05715684 |
| Optical Coherence Tomography (OCT) | Other | Approved | In-stent Restenosis | COMPLETED | NCT04268875 |
| Optical Coherence Tomography (OCT) | Other | Approved | In-stent Restenosis | COMPLETED | NCT04268875 |
| Optical Coherence Tomography (OCT) | Other | Approved | In-stent Restenosis | COMPLETED | NCT04268875 |
| Optical Coherence Tomography (OCT) | Other | Approved | In-stent Restenosis | COMPLETED | NCT04268875 |
| FreeStyle Precision Neo blood glucose meter | Other | Approved | Diabetes Mellitus, Type 2 | UNKNOWN | NCT05822232 |
| FreeStyle Libre Pro blinded CGM | Other | Approved | Diabetes Mellitus, Type 2 | UNKNOWN | NCT05822232 |
| FreeStyle Libre 2 CGM | Other | Approved | Diabetes Mellitus, Type 2 | UNKNOWN | NCT05822232 |
| NxTekTM Malaria Pf Plus Rapid Diagnostic Test Device | Device | Approved | Malaria | COMPLETED | NCT05286359 |
| NxTekTM Malaria Pf Plus Rapid Diagnostic Test Device | Device | Approved | Malaria | COMPLETED | NCT05286359 |
| ANS Totally Implantable Deep Brain Stimulation System | Other | Approved | Tremor | COMPLETED | NCT02087046 |
| ANS Totally Implantable Deep Brain Stimulation System | Other | Approved | Tremor | COMPLETED | NCT02087046 |
| New York Heart Association Classification Guide | Other | Approved | Heart Failure | UNKNOWN | NCT05833581 |
| New York Heart Association Classification Guide | Other | Approved | Heart Failure | UNKNOWN | NCT05833581 |
| Valproic Acid | Other | Phase PHASE1 | Spinal Muscular Atrophy | COMPLETED | NCT00374075 |
| Itraconazole | Other | Phase PHASE1 | Tinea Versicolor | COMPLETED | NCT05862714 |
| Fluconazole | Other | Phase PHASE1 | Tinea Versicolor | COMPLETED | NCT05862714 |
| Itraconazole | Other | Phase PHASE1 | Tinea Versicolor | COMPLETED | NCT05862714 |
| Fluconazole | Other | Phase PHASE1 | Tinea Versicolor | COMPLETED | NCT05862714 |
| Sulphur | Other | Phase PHASE1 | Scabies | COMPLETED | NCT05862701 |
| Permethrin | Other | Phase PHASE1 | Scabies | COMPLETED | NCT05862701 |
| Sulphur | Other | Phase PHASE1 | Scabies | COMPLETED | NCT05862701 |
| Permethrin | Other | Phase PHASE1 | Scabies | COMPLETED | NCT05862701 |
| MPP | Other | Approved | Heart Failure | TERMINATED | NCT02006069 |
| MPP | Other | Approved | Heart Failure | TERMINATED | NCT02006069 |
| Platelets rich plasma | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05884151 |
| Tranexamic acid | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05884151 |
| Platelets rich plasma | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05884151 |
| Tranexamic acid | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05884151 |
| Group B Azelaic Acid 20 % Cream for 6 months | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Group A 4 % Hydroquinone Cream Topically and Oral Tranexamic Acid | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Group B Azelaic Acid 20 % Cream for 6 months | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Group A 4 % Hydroquinone Cream Topically and Oral Tranexamic Acid | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Group B Azelaic Acid 20 % Cream for 6 months | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Group A 4 % Hydroquinone Cream Topically and Oral Tranexamic Acid | Other | Phase PHASE1 | Melasma | COMPLETED | NCT05887219 |
| Biventricular pacemaker | Other | Approved | Diastolic Heart Failure | COMPLETED | NCT03338374 |
| Biventricular pacemaker | Other | Approved | Diastolic Heart Failure | COMPLETED | NCT03338374 |
| Liquid nitrogen | Other | Phase PHASE1 | Plan Warts | COMPLETED | NCT05895071 |
| 5%potassium hydroxide | Other | Phase PHASE1 | Plan Warts | COMPLETED | NCT05895071 |
| Liquid nitrogen | Other | Phase PHASE1 | Plan Warts | COMPLETED | NCT05895071 |
| 5%potassium hydroxide | Other | Phase PHASE1 | Plan Warts | COMPLETED | NCT05895071 |
| Group B received 10% Potassium Hydroxide Solution | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05897112 |
| Group A received cryotherpay | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05897112 |
| Group B received 10% Potassium Hydroxide Solution | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05897112 |
| Group A received cryotherpay | Other | Phase PHASE1 | Molluscum Contagiosum | COMPLETED | NCT05897112 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| OCT guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Angiographic guided PCI | Other | Approved | Ischaemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03171311 |
| Amplatzer Cardiac Plug | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT01786486 |
| T-Wave Alternans test | Other | Phase PHASE3 | Ischemic Cardiomyopathy | COMPLETED | NCT00187291 |
| T-Wave Alternans test | Other | Phase PHASE3 | Ischemic Cardiomyopathy | COMPLETED | NCT00187291 |
| Cardiac Ablation (Gen2 Cardiac Ablation System) | Other | Approved | Atrial Flutter | TERMINATED | NCT00606463 |
| Diamondback 360 Extended Length Orbital Atherectomy System | Other | Preclinical | Peripheral Artery Disease | COMPLETED | NCT03943160 |
| 014 Drug Coated Balloon | Drug | Approved | PAD | COMPLETED | NCT02561299 |
| Peripheral Orbital Atherectomy System | Other | Approved | PAD | COMPLETED | NCT02561299 |
| Coronary Orbital Atherectomy plus Stenting | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT02339545 |
| Diamondback 360® Coronary OAS Micro Crown | Other | Approved | CAD | COMPLETED | NCT02132611 |
| Diamondback 360® Coronary OAS Micro Crown | Other | Approved | CAD | COMPLETED | NCT02132611 |
| Stealth 360°® OAS | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT01938391 |
| Percutaneous Coronary Intervention | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT01930214 |
| PAD endovascular treatments | Drug | Preclinical | Peripheral Arterial Occlusive Disease | COMPLETED | NCT01855412 |
| Perclose ProGlide SMC System and/or Perclose ProStyle SMCR System | Other | Approved | Arrhythmia | COMPLETED | NCT04904809 |
| Abbott Infinity DBS systems with the NeuroSphere Virtual Clinic feature (virtual clinic and in-clinic sessions) | Other | Approved | Parkinson Disease | ACTIVE_NOT_RECRUITING | NCT05269862 |
| Abbott Infinity DBS systems with the NeuroSphere Virtual Clinic feature | Other | Approved | Parkinson Disease | ACTIVE_NOT_RECRUITING | NCT05269862 |
| FreeStyle Libre 2 System | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT04604093 |
| SMBG Meter | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT04604093 |
| HeartMate PHP | Other | Approved | Cardiogenic Shock | TERMINATED | NCT02279979 |
| Patient Advisory Module | Other | Approved | Heart Failure | COMPLETED | NCT01121107 |
| Left Atrial Pressure Monitoring System | Other | Approved | Heart Failure | COMPLETED | NCT01121107 |
| FreeStyle Libre 3 | Other | Preclinical | Diabetes Mellitus | TERMINATED | NCT05962710 |
| DRG Stimulator | Other | Approved | Chronic Pain | COMPLETED | NCT03908476 |
| Burst-capable SCS system | Other | Approved | Chronic Pain | COMPLETED | NCT03908476 |
| Progestagen | Other | Preclinical | Early Pregnancy Bleeding | TERMINATED | NCT05186779 |
| Progestagen | Other | Preclinical | Early Pregnancy Bleeding | TERMINATED | NCT05186779 |
| Electrophysiological study and bi-atrial Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study and Right side Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study and bi-atrial Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study and Right side Ganglionated Plexi ablation | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Electrophysiological study | Other | Approved | Bradycardia; Syncope | UNKNOWN | NCT05572034 |
| Abbott SCS Systems | Other | Preclinical | Chronic Pain | COMPLETED | NCT05659836 |
| Balloon | Other | Approved | Coronary Artery Disease | UNKNOWN | NCT03108456 |
| Orbital Atherectomy | Other | Approved | Coronary Artery Disease | UNKNOWN | NCT03108456 |
| Implantable spinal cord stimulator | Other | Preclinical | Complex Regional Pain Syndrome Type I | UNKNOWN | NCT05877612 |
| Implantable spinal cord stimulator | Other | Preclinical | Complex Regional Pain Syndrome Type I | RECRUITING | NCT05877612 |
| TactiCath SE | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03354663 |
| TactiCath SE | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03354663 |
| XIENCE | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01751906 |
| Absorb BVS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01751906 |
| Breakfast 2 | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT05802927 |
| Breakfast 1 | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT05802927 |
| DSF | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT05802927 |
| XIENCE | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02173379 |
| Absorb BVS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02173379 |
| XIENCE | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02173379 |
| Absorb BVS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02173379 |
| TactiFlex SE - High Standard Power | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT04356040 |
| TactiFlex SE | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT04356040 |
| BurstDR-SCS | Other | Approved | Chronic Intractable Pain | WITHDRAWN | NCT06030284 |
| BurstDR-SCS | Other | Approved | Chronic Intractable Pain | WITHDRAWN | NCT06030284 |
| Usual Care | Other | Approved | Heart Failure | COMPLETED | NCT04942353 |
| Home-based Exercise Rehabilitation. | Other | Approved | Heart Failure | COMPLETED | NCT04942353 |
| Diabetes self-management education | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04562714 |
| FreeStyle Libre Flash Glucose Monitor | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04562714 |
| Panbio™ | Other | Approved | COVID-19 | COMPLETED | NCT05630365 |
| Nasal and Nasopharyngeal Sampling of the Panbio™ COVID-19/ Flu A&B Rapid Panel | Other | Approved | COVID-19 | COMPLETED | NCT05354115 |
| MINI TREK RX 1.20 mm Coronary Dilatation Catheter | Other | Preclinical | Ischemic Heart Disease | COMPLETED | NCT01186198 |
| Trifecta™ aortic bioprosthesis | Other | Preclinical | Aortic Valve Disease | TERMINATED | NCT01256710 |
| Trifecta™ aortic bioprosthesis | Other | Preclinical | Aortic Valve Disease | TERMINATED | NCT01256710 |
| Racecadotril plus ORS | Other | Phase PHASE3 | Diarrhea, Infantile | COMPLETED | NCT03473561 |
| Racecadotril plus ORS | Other | Phase PHASE3 | Diarrhea, Infantile | COMPLETED | NCT03473561 |
| Study MRI scan | Other | Preclinical | Tachycardia | COMPLETED | NCT03828357 |
| Thoracic MRI Scan | Other | Approved | ICD | COMPLETED | NCT02877693 |
| CSI pVAD system | Other | Approved | Coronary Artery Disease | COMPLETED | NCT05315544 |
| Intravascular lithotripsy (IVL) | Other | Approved | Calcified Coronary Artery Disease | UNKNOWN | NCT05072730 |
| Super High Pressure Balloon (OPN NC) | Other | Approved | Calcified Coronary Artery Disease | UNKNOWN | NCT05072730 |
| CRT+NAVH | Other | Preclinical | Heart Failure | COMPLETED | NCT02903940 |
| CRT+NAVH | Other | Preclinical | Heart Failure | COMPLETED | NCT02903940 |
| CRT+NAVH | Other | Preclinical | Heart Failure | COMPLETED | NCT02782598 |
| CRT+NAVH | Other | Preclinical | Heart Failure | COMPLETED | NCT02782598 |
| CSI pVAD System | Other | Approved | Coronary Artery Disease | WITHDRAWN | NCT05695716 |
| CGM device with diabetic education, CGM education and a follow up protocol. | Device | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT04729985 |
| CGM device with diabetic education, CGM education and a follow up protocol. | Device | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT04729985 |
| Control Product | Other | Approved | Gastrointestinal Cancer | COMPLETED | NCT05301556 |
| Experimental Product | Other | Approved | Gastrointestinal Cancer | COMPLETED | NCT05301556 |
| Routinely performed echo, ECG and hemodynamic monitoring | Other | Preclinical | End-stage Heart Failure | RECRUITING | NCT04641416 |
| Catheter ablation | Other | Preclinical | Paroxysmal Atrial Fibrillation | COMPLETED | NCT04022954 |
| EverFlex™ Self-Expanding Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | UNKNOWN | NCT03941314 |
| Supera® Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | UNKNOWN | NCT03941314 |
| EverFlex™ Self-Expanding Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | ACTIVE_NOT_RECRUITING | NCT03941314 |
| Supera® Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | ACTIVE_NOT_RECRUITING | NCT03941314 |
| AMPLATZER™ LAA Occluder | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT02964208 |
| CTI line | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Voltage | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Wave Speed | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Confluent areas | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| CTI line | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Voltage | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Wave Speed | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Confluent areas | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| CTI line | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Voltage | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Wave Speed | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| Confluent areas | Other | Approved | Flutter | RECRUITING | NCT05709795 |
| XIENCE PRIME SV Everolimus Eluting Coronary Stent | Other | Preclinical | Ischemic Heart Disease | COMPLETED | NCT02513719 |
| Deep Brain Stimulation, Libra Deep Brain Stimulation System | Other | Approved | Depressive Disorder, Major | TERMINATED | NCT00617162 |
| Advisor HD Grid Mapping Catheter, Sensor Enabled | Other | Preclinical | Persistent Atrial Fibrillation | COMPLETED | NCT03733392 |
| CardioMEMS HF System | Other | Preclinical | Heart Failure | COMPLETED | NCT02279888 |
| Transcatheter Aortic Valve Implantation | Other | Preclinical | Bicuspid Aortic Valve | NOT_YET_RECRUITING | NCT06375590 |
| Transcatheter Aortic Valve Implantation | Other | Preclinical | Bicuspid Aortic Valve | NOT_YET_RECRUITING | NCT06375590 |
| Deferred stenting | Other | Approved | Acute Myocardial Infarction With ST Elevation | ACTIVE_NOT_RECRUITING | NCT03744000 |
| Immediate stenting | Other | Approved | Acute Myocardial Infarction With ST Elevation | ACTIVE_NOT_RECRUITING | NCT03744000 |
| Deferred stenting | Other | Approved | Acute Myocardial Infarction With ST Elevation | ACTIVE_NOT_RECRUITING | NCT03744000 |
| Immediate stenting | Other | Approved | Acute Myocardial Infarction With ST Elevation | ACTIVE_NOT_RECRUITING | NCT03744000 |
| Panbio™ | Other | Approved | COVID-19 | COMPLETED | NCT06127108 |
| Hemodynamic management using CardioMEMS HF System | Other | Preclinical | Heart Failure | COMPLETED | NCT03247829 |
| Hydrolyzed protein infant formula with oligosaccharides | Other | Approved | Gastrointestinal Tolerance | COMPLETED | NCT05369494 |
| ID NOW™ | Other | Approved | Chlamydia Trachomatis Infection | NOT_YET_RECRUITING | NCT06395675 |
| Cellulose Based (Losartan Placebo) | Other | Phase PHASE2 | Inflammation | COMPLETED | NCT02676466 |
| Corn Oil (Fish oil Placebo) | Other | Phase PHASE2 | Inflammation | COMPLETED | NCT02676466 |
| Losartan | Other | Phase PHASE2 | Inflammation | COMPLETED | NCT02676466 |
| Omega-3 fish oil | Other | Phase PHASE2 | Inflammation | COMPLETED | NCT02676466 |
| HP-SD AF ablation by a CF sensing catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05758805 |
| mini-invasive esophagoscopy | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05758805 |
| HP-SD AF ablation by a CF sensing catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05758805 |
| mini-invasive esophagoscopy | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05758805 |
| Burst SCS Stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Tonic SCS stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Sham SCS stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Burst SCS Stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Tonic SCS stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Sham SCS stimulation | Other | Approved | Spinal Cord Stimulation (SCS) | COMPLETED | NCT04272411 |
| Medical Therapy | Drug | Approved | Ventricular Remodeling, Left | TERMINATED | NCT03891823 |
| MitraClip | Other | Approved | Ventricular Remodeling, Left | TERMINATED | NCT03891823 |
| Medical Therapy | Drug | Approved | Ventricular Remodeling, Left | TERMINATED | NCT03891823 |
| MitraClip | Other | Approved | Ventricular Remodeling, Left | TERMINATED | NCT03891823 |
| MPP + SyncAV | Other | Preclinical | Cardiac Resynchronization Therapy | COMPLETED | NCT06444386 |
| Medical Therapy | Drug | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT02830152 |
| LAAO | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT02830152 |
| FreeStyle Navigator Continuous Glucose Monitoring System Version 1.5 | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT01076218 |
| HeartMate 3™ left ventricular assist system (HM3 LVAS) | Other | Approved | Advanced Heart Failure | TERMINATED | NCT04703855 |
| SJM Infinity™ DBS IPG or SJM Brio™ DBS IPG system | Other | Preclinical | Parkinson Disease | COMPLETED | NCT02963259 |
| SJM Infinity™ DBS IPG or SJM Brio™ DBS IPG system | Other | Preclinical | Parkinson Disease | COMPLETED | NCT02963259 |
| Dorsal Root Ganglion (DRG) Stimulation (Proclaim™ Neurostimulator System) | Other | Preclinical | Complex Regional Pain Syndrome (CRPS) | COMPLETED | NCT02800863 |
| Dorsal Root Ganglion (DRG) Stimulation (Axium™ Neurostimulator System) | Other | Preclinical | Complex Regional Pain Syndrome (CRPS) | COMPLETED | NCT02800863 |
| Burst and Tonic stimulation | Other | Approved | Chronic Pain | COMPLETED | NCT02143791 |
| Standard of care neuromodulation therapy (SCS or DRG) | Drug | Approved | Chronic Pain | RECRUITING | NCT05537662 |
| JETi 6F and 8F Thrombectomy system | Other | Approved | Peripheral Arterial Disease | NOT_YET_RECRUITING | NCT06434779 |
| JETi 6F and 8F Thrombectomy system | Other | Approved | Peripheral Arterial Disease | NOT_YET_RECRUITING | NCT06434779 |
| Observation / Data Collection | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT03041233 |
| Observation / Data Collection | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT03041233 |
| MitraClip NT System | Other | Preclinical | Mitral Regurgitation | COMPLETED | NCT03500692 |
| MitraClip NT System | Other | Preclinical | Mitral Regurgitation | COMPLETED | NCT03500692 |
| HeartMate 3™ left ventricular assist system (HM3 LVAS) | Other | Approved | Advanced Heart Failure | COMPLETED | NCT04915924 |
| HeartMate 3™ left ventricular assist system (HM3 LVAS) | Other | Approved | Advanced Heart Failure | COMPLETED | NCT04915924 |
| Control Polyunsaturated Oil Blend | Other | Approved | Nutrition, Healthy | COMPLETED | NCT06266702 |
| Experimental Oil with Phospholipids | Other | Approved | Nutrition, Healthy | COMPLETED | NCT06266702 |
| Coronary PCI guided by Angiography | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03507777 |
| Coronary PCI guided by OCT | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03507777 |
| Radiofrequency Ablation | Other | Preclinical | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03906461 |
| ABSORB GT1 BVS | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT03409731 |
| ABSORB GT1 BVS | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT03409731 |
| Panbio™ COVID-19/Flu A&B Panel | Other | Approved | COVID-19 | COMPLETED | NCT06124638 |
| Panbio™ COVID-19/Flu A&B Panel | Other | Approved | COVID-19 | COMPLETED | NCT06124638 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05270499 |
| Diagnostic test: Determine™ Syphilis Advanced test | Other | Approved | Syphilis Infection | NOT_YET_RECRUITING | NCT06584214 |
| Diagnostic test: Determine™ Syphilis Advanced test | Other | Approved | Syphilis Infection | NOT_YET_RECRUITING | NCT06584214 |
| i-STAT hs-TnI Cartridge Testing on i-STAT 1 and i-STAT Alinity | Other | Preclinical | Myocardial Infarction | COMPLETED | NCT05629572 |
| Water | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| Oral Rehydration Solution | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| Control Group | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| Water | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| Oral Rehydration Solution | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| Control Group | Other | Approved | Hydration | TERMINATED | NCT05569044 |
| A specific electrophysiology mapping protocol is applicable with the GRID catheter. | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03882021 |
| A specific electrophysiology mapping protocol is applicable with the GRID catheter. | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03882021 |
| FIRM-Guided Procedure and PVI | Procedure | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT02799043 |
| Standard PVI | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT02799043 |
| Dorsal root ganglion (DRG) stimulation | Other | Approved | Chronic Pain | COMPLETED | NCT02587637 |
| Panbio™ HCV Self Test | Other | Approved | HEPATITIS C (HCV) | NOT_YET_RECRUITING | NCT06605573 |
| FreeStyle Libre 2 Flash Glucose Monitoring System | Other | Approved | Type 2 Diabetes Treated With Insulin | TERMINATED | NCT06268821 |
| Pacemaker Implantation | Other | Approved | Bradycardia | COMPLETED | NCT01912326 |
| Pacemaker Implantation | Other | Approved | Bradycardia | COMPLETED | NCT01912326 |
| no intervention | Other | Preclinical | Aortic Valve Disease | COMPLETED | NCT05389631 |
| no intervention | Other | Preclinical | Aortic Valve Disease | COMPLETED | NCT05389631 |
| no intervention | Other | Preclinical | Aortic Valve Disease | COMPLETED | NCT05389631 |
| AMPLATZER™ Post-infarct Muscular VSD Occluder | Other | Preclinical | Post-Infarction Ventricular Septal Defect | COMPLETED | NCT03165526 |
| Portico™ Valve, FlexNav Delivery System(s) and Loading System(s) | Other | Approved | Symptomatic Degenerative Aortic Stenosis | COMPLETED | NCT03752866 |
| Portico™ Valve, Portico Delivery System(s) and Loading System(s) | Other | Approved | Symptomatic Degenerative Aortic Stenosis | COMPLETED | NCT03752866 |
| Ensure Plus Advance | Other | Approved | Sarcopenia | COMPLETED | NCT05344313 |
| Ensure Plus Advance | Other | Approved | Sarcopenia | COMPLETED | NCT05344313 |
| Ensure Plus Advance | Other | Approved | Sarcopenia | COMPLETED | NCT05344313 |
| Systematic etiologic work-up for underlying causes of MINOCA | Other | Preclinical | MINOCA | RECRUITING | NCT05326828 |
| CONFIRM Rx implantable cardiac rhythm monitor (Abbott) | Other | Preclinical | MINOCA | RECRUITING | NCT05326828 |
| Amplatzer PFO Occluder | Other | Preclinical | PFO - Patent Foramen Ovale | ACTIVE_NOT_RECRUITING | NCT04349995 |
| Tricuspid Valve Repair System | Other | Approved | Tricuspid Valve Insufficiency | COMPLETED | NCT03227757 |
| LVAD implant | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT04865978 |
| Warfarin | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT04865978 |
| Apixaban | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT04865978 |
| Implantation with the commercially available Axium Neurostimulator | Other | Preclinical | Chronic Pain | COMPLETED | NCT02169401 |
| Deep Brain Stimulation | Other | Approved | Depressive Disorder, Major | COMPLETED | NCT01331330 |
| Tendyne Mitral Valve System | Other | Approved | Mitral Regurgitation | COMPLETED | NCT03539458 |
| Neurostimulation | Other | Approved | Discogenic Pain | COMPLETED | NCT03958604 |
| IonicRF Generator and compatible accessories | Other | Preclinical | Pain | COMPLETED | NCT04873817 |
| IonicRF Generator and compatible accessories | Other | Preclinical | Pain | COMPLETED | NCT04873817 |
| Infinity DBS System with MR Conditional labelling | Other | Preclinical | Movement Disorders | COMPLETED | NCT03884231 |
| Infinity DBS System with MR Conditional labelling | Other | Preclinical | Movement Disorders | COMPLETED | NCT03884231 |
| Panbio™ HCV Self Test | Other | Preclinical | Hepatitis C | NOT_YET_RECRUITING | NCT06492018 |
| Panbio™ HCV Self Test | Other | Preclinical | Hepatitis C | NOT_YET_RECRUITING | NCT06492018 |
| Pulmonary artery OCT | Other | Preclinical | Pulmonary Hypertension | COMPLETED | NCT05843461 |
| Right Ventricle Index of Microcirculatory Resistance | Other | Preclinical | Pulmonary Hypertension | COMPLETED | NCT05843461 |
| Pulmonary Index of Microcirculatory Resistance | Other | Preclinical | Pulmonary Hypertension | COMPLETED | NCT05843461 |
| CentriMag Circulatory Support System | Other | Preclinical | Heart Failure | COMPLETED | NCT04464785 |
| CardioMEMS | Other | Approved | Heart Failure | WITHDRAWN | NCT04977310 |
| CardioMEMS | Other | Approved | Heart Failure | WITHDRAWN | NCT04977310 |
| Drug coated ballloon (DCB) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Drug eluting stent (DES) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Drug coated ballloon (DCB) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Drug eluting stent (DES) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Drug coated ballloon (DCB) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Drug eluting stent (DES) | Drug | Approved | Coronary Artery Disease | RECRUITING | NCT05544864 |
| Transcatheter heart valve procedure | Procedure | Preclinical | Tricuspid Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04483089 |
| ABT NG DES 48 EECSS | Other | Approved | Coronary Artery Disease | COMPLETED | NCT04282148 |
| ConfirmRx (Insertable Cardiac Monitor) | Other | Approved | Syncope | COMPLETED | NCT03803969 |
| ConfirmRx (Insertable Cardiac Monitor) | Other | Approved | Syncope | COMPLETED | NCT03803969 |
| To utilize the FreeStyle Libre 3 Continuous Glucose Monitoring System (FSL3) to help prolong the length of time people with diabetes maintain adherence to GLP-1 and dual GIP/GLP-1 agonists | Other | Preclinical | Diabetes Mellitus | RECRUITING | NCT06668935 |
| To utilize the FreeStyle Libre 3 Continuous Glucose Monitoring System (FSL3) to help prolong the length of time people with diabetes maintain adherence to GLP-1 and dual GIP/GLP-1 agonists | Other | Preclinical | Diabetes Mellitus | RECRUITING | NCT06668935 |
| Continuous Glucose Monitoring | Other | Preclinical | Cardiometabolic Risk Factors | ENROLLING_BY_INVITATION | NCT06790472 |
| Online Lifestyle Intervention | Other | Preclinical | Cardiometabolic Risk Factors | ENROLLING_BY_INVITATION | NCT06790472 |
| FreeStyle Libre 2 Flash Glucose Monitoring System | Other | Preclinical | Diabetes Mellitus, Type 2 | TERMINATED | NCT05168306 |
| FreeStyle Libre System plus food app | Other | Approved | Diabetes Mellitus, Type 2 | UNKNOWN | NCT04843527 |
| FreeStyle Libre System | Other | Approved | Diabetes Mellitus, Type 2 | UNKNOWN | NCT04843527 |
| Conventional Medical Management | Other | Approved | Chronic Low-Back Pain | COMPLETED | NCT04479787 |
| Spinal Cord Stimulation | Other | Approved | Chronic Low-Back Pain | COMPLETED | NCT04479787 |
| Aquify MPS | Other | Approved | Myopia | WITHDRAWN | NCT01019564 |
| Complete Easy Rub Formula MPS | Other | Approved | Myopia | WITHDRAWN | NCT01019564 |
| Systane | Other | Phase PHASE2 | Dry Eye | COMPLETED | NCT00607776 |
| (9587X) Blink Tears, classified as an OTC Drug with the active ingredient being plyethylene glycol 400 | Drug | Phase PHASE2 | Dry Eye | COMPLETED | NCT00607776 |
| PCI revascularization strategy based FFR assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| PCI revascularization strategy based on combined FFR and OCT assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| PCI revascularization strategy based FFR assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| PCI revascularization strategy based on combined FFR and OCT assessment | Other | Approved | Multivessel Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05333068 |
| STAR S4 IR laser with iDesign | Other | Approved | Stable Myopic Refractive Error, With or Without Astigmatism | COMPLETED | NCT02675751 |
| STAR S4 IR laser with iDesign | Other | Approved | Stable Myopic Refractive Error, With or Without Astigmatism | COMPLETED | NCT02675751 |
| TECNIS Toric Models ZCT450, ZCT525 or ZCT600 | Other | Approved | Cataract | COMPLETED | NCT02649842 |
| TECNIS Toric Models ZCT450, ZCT525 or ZCT600 | Other | Approved | Cataract | COMPLETED | NCT02649842 |
| iFS Femtosecond Laser | Other | Approved | Cataract | COMPLETED | NCT01713660 |
| iFS Femtosecond Laser | Other | Approved | Cataract | COMPLETED | NCT01713660 |
| LASIK | Other | Approved | Astigmatism | COMPLETED | NCT01675492 |
| One-Piece Tecnis monofocal IOL, Model ZCB00 | Other | Phase PHASE4 | Cataract | COMPLETED | NCT01210807 |
| One-Piece Tecnis Multifocal IOL | Other | Phase PHASE4 | Cataract | COMPLETED | NCT01210807 |
| FS Laser System | Other | Approved | Cataract | TERMINATED | NCT00922571 |
| FS Laser Surgery | Procedure | Approved | Cataract | TERMINATED | NCT00922571 |
| CeeOn 911A monofocal IOL | Other | Approved | Cataract | COMPLETED | NCT00747565 |
| Tecnis ZM900 Multifocal Intraocular Lens | Other | Approved | Cataract | COMPLETED | NCT00747565 |
| Subclavian /Axillary TAVR implant | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT03056573 |
| Transaortic TAVR Implant | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT03056573 |
| ADO II AS (PDA closure) | Other | Approved | Patent Ductus Arteriosus | COMPLETED | NCT03055858 |
| Trifecta GT (Glide Technology) Valve | Other | Approved | Aortic Valve Disease | COMPLETED | NCT03016169 |
| Mitral valve replacement SJM™ Masters HP™ 15mm Rotatable Mechanical Heart Valve | Other | Approved | Mitral Valve Disease | COMPLETED | NCT02097420 |
| Mitral valve replacement SJM™ Masters HP™ 15mm Rotatable Mechanical Heart Valve | Other | Approved | Mitral Valve Disease | COMPLETED | NCT02097420 |
| Transcatheter Aortic Valve Implant | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT01802788 |
| St Jude Medical Portico replacement aortic valve | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT01802788 |
| Trifecta™ Valve | Other | Preclinical | Aortic Valve Insufficiency | COMPLETED | NCT01593917 |
| Viscoat | Other | Approved | Cataract | COMPLETED | NCT00972621 |
| Vitrax II | Other | Approved | Cataract | COMPLETED | NCT00972621 |
| Viscoat | Other | Approved | Cataract | COMPLETED | NCT00972621 |
| Vitrax II | Other | Approved | Cataract | COMPLETED | NCT00972621 |
| Muscular VSD Occluder device implantation (AMPLATZER Muscular VSD Occluder) | Device | Approved | Ventricular Septal Defects | COMPLETED | NCT00647387 |
| Muscular VSD Occluder device implantation (AMPLATZER Muscular VSD Occluder) | Device | Approved | Ventricular Septal Defects | COMPLETED | NCT00647387 |
| ABT-888 | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| Temozolomide | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| ABT-888 | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| Temozolomide | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| ABT-888 | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| Temozolomide | Other | Phase PHASE2 | Hepatocellular Carcinoma | TERMINATED | NCT01205828 |
| Protein supplement | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| β-hydroxy β-methylbutyrate (HMB) supplement | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| Low-magnitude High-frequency Vibration | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| Protein supplement | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| β-hydroxy β-methylbutyrate (HMB) supplement | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| Low-magnitude High-frequency Vibration | Other | Approved | Sarcopenia | RECRUITING | NCT05525039 |
| post-PCI Pd/Pa | Other | Approved | Percutaneous Coronary Revascularisation | RECRUITING | NCT04780971 |
| post-PCI Pd/Pa | Other | Approved | Percutaneous Coronary Revascularisation | RECRUITING | NCT04780971 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | ACTIVE_NOT_RECRUITING | NCT06172699 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | ACTIVE_NOT_RECRUITING | NCT06172699 |
| Patient Preference Survey | Other | Preclinical | Cardiac Rhythm Disorder | COMPLETED | NCT05327101 |
| Patient Preference Survey | Other | Preclinical | Cardiac Rhythm Disorder | COMPLETED | NCT05327101 |
| LBBAP with SyncAV | Other | Preclinical | Heart Failure | RECRUITING | NCT06436053 |
| Commercially available transcatheter aortic valve | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02000115 |
| Portico transcatheter aortic valve | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02000115 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Pulsed Field Ablation | Other | Approved | Paroxysmal AF | RECRUITING | NCT07181590 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Holter monitoring in patients who have been successfully implanted with an Abbott Assert-IQ ICM device | Device | Preclinical | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06172699 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Intravascular imaging (OCT), Invasive physiologic assessment (FFR, CFR, IMR), or Non-invasive physiologic assessment (N-13 ammonia PET) | Other | Preclinical | Myocardial Infarction | RECRUITING | NCT05272618 |
| VFR Analysis | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| FFR | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| OCT | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| ICA (Invasive Coronary Angiography) | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| VFR Analysis | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| FFR | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| OCT | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| ICA (Invasive Coronary Angiography) | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT04356027 |
| LV only pacing with MPP and SyncAV | Other | Approved | Heart Failure | COMPLETED | NCT03567096 |
| BiV pacing with MPP and SyncAV | Other | Approved | Heart Failure | COMPLETED | NCT03567096 |
| LV only pacing with MPP and SyncAV | Other | Approved | Heart Failure | COMPLETED | NCT03567096 |
| BiV pacing with MPP and SyncAV | Other | Approved | Heart Failure | COMPLETED | NCT03567096 |
| Intravascular imaging (OCT), Invasive physiologic assessment (FFR, CFR, IMR), or Non-invasive physiologic assessment (N-13 ammonia PET) | Other | Preclinical | Myocardial Infarction | RECRUITING | NCT05272618 |
| CardioMEMS HF System | Other | Preclinical | Heart Failure | COMPLETED | NCT02954341 |
| WATCHMAN Left Atrial Appendage Closure | Other | Approved | Stroke | COMPLETED | NCT02879448 |
| Amulet Left Atrial Appendage Occluder | Other | Approved | Stroke | COMPLETED | NCT02879448 |
| Water | Other | Approved | Dehydration | TERMINATED | NCT06368765 |
| Oral Rehydration Solution (ORS) | Other | Approved | Dehydration | TERMINATED | NCT06368765 |
| Transcatheter Aortic Valve Replacement | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT05002088 |
| Investigational device | Device | Approved | Bilateral Vocal Fold Paralysis (BVFP) | TERMINATED | NCT03085316 |
| Investigational MPS | Other | Approved | Corneal Staining | COMPLETED | NCT01240122 |
| Biotrue MPS | Other | Approved | Corneal Staining | COMPLETED | NCT01240122 |
| Investigational MPS | Other | Approved | Corneal Staining | COMPLETED | NCT01240122 |
| Biotrue MPS | Other | Approved | Corneal Staining | COMPLETED | NCT01240122 |
| temozolomide | Other | Phase PHASE2 | Breast Cancer | COMPLETED | NCT01009788 |
| ABT-888 | Other | Phase PHASE2 | Breast Cancer | COMPLETED | NCT01009788 |
| Lopinavir/ritonavir with two nucleoside analogs | Other | Phase PHASE4 | HIV/HCV Co-infection | COMPLETED | NCT00866021 |
| Lopinavir/ritonavir | Other | Phase PHASE4 | HIV/HCV Co-infection | COMPLETED | NCT00866021 |
| Lopinavir/ritonavir with two nucleoside analogs | Other | Phase PHASE4 | HIV/HCV Co-infection | COMPLETED | NCT00866021 |
| Lopinavir/ritonavir | Other | Phase PHASE4 | HIV/HCV Co-infection | COMPLETED | NCT00866021 |
| Fingerstick blood draw | Other | Approved | Potassium (K) & Ionized Calcium (iCa) in Capillary Whole Blood | COMPLETED | NCT06295835 |
| Placebo | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00227266 |
| Valproic Acid and Levocarnitine | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00227266 |
| Placebo | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00227266 |
| Valproic Acid and Levocarnitine | Other | Phase PHASE2 | Spinal Muscular Atrophy | COMPLETED | NCT00227266 |
| Continuous Glucose Monitoring (CGM) | Other | Approved | Type 2 Diabetes | COMPLETED | NCT05516797 |
| Echocardiogram, cardiac | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Responsive Management Intervention | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Percutaneous Patent Ductus Arteriosus Closure (PPC) | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Echocardiogram, cardiac | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Responsive Management Intervention | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Percutaneous Patent Ductus Arteriosus Closure (PPC) | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Echocardiogram, cardiac | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Responsive Management Intervention | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Percutaneous Patent Ductus Arteriosus Closure (PPC) | Other | Approved | Ductus Arteriosus, Patent | RECRUITING | NCT05547165 |
| Single-chamber atrial transvenous pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT06100770 |
| Aveir AR Leadless Pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT06100770 |
| Single-chamber atrial transvenous pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT06100770 |
| Aveir AR Leadless Pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT06100770 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05935007 |
| Dual Chamber Transvenous Pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05932602 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05932602 |
| Dual Chamber Transvenous Pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05932602 |
| Aveir DR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05932602 |
| AVEIR remote care system | Other | Preclinical | Cardiac Pacemaker | COMPLETED | NCT06542133 |
| BinaxNOW™ COVID-19/Flu A&B Combo Self-Test | Other | Approved | Influenza Type A | NOT_YET_RECRUITING | NCT06928129 |
| High Density Voltage Mapping | Other | Approved | Sustained Monomorphic VT (MMVT) | NOT_YET_RECRUITING | NCT06931821 |
| Isochronal Late Activation Mapping (ILAM) | Other | Approved | Sustained Monomorphic VT (MMVT) | NOT_YET_RECRUITING | NCT06931821 |
| Drug-eluting stent | Drug | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Angiography-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| OCT-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Drug-eluting stent | Drug | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Angiography-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| OCT-guided PCI | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05493904 |
| Dydrogesterone | Other | Preclinical | Endometriosis | NOT_YET_RECRUITING | NCT06952296 |
| Dydrogesterone | Other | Preclinical | Endometriosis | NOT_YET_RECRUITING | NCT06952296 |
| Digital Subtraction Angiography | Other | Preclinical | Peripheral Artery Disease | COMPLETED | NCT04748965 |
| Intensification of diabetes medication based on glucose levels | Drug | Approved | Type 2 Diabetes | ACTIVE_NOT_RECRUITING | NCT05040087 |
| Intensification of diabetes medication based largely on HbA1c levels | Drug | Approved | Type 2 Diabetes | ACTIVE_NOT_RECRUITING | NCT05040087 |
| Open loop | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT06959797 |
| Closed loop | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT06959797 |
| Fixed Pulse Width | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT03632057 |
| Fixed Tilt (65%) | Other | Approved | Ventricular Arrythmia | COMPLETED | NCT03632057 |
| Continuous glucose monitoring | Other | Approved | Type 2 Diabetes Mellitus (T2DM) | RECRUITING | NCT06888687 |
| Dietetic support | Other | Approved | Type 2 Diabetes Mellitus (T2DM) | RECRUITING | NCT06888687 |
| MRI/ CardioMEMS comparison | Other | Preclinical | Heart Failure | COMPLETED | NCT05428384 |
| HBA1c data and glucose levels | Other | Preclinical | Diabetes Mellitus | COMPLETED | NCT05189938 |
| Placebo Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| Experimental Extensively Hydrolyzed Formula | Other | Approved | Cow's Milk Allergy | RECRUITING | NCT06456541 |
| LIBERATE | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05261906 |
| LIBERATE | Other | Approved | Diabetes Mellitus, Type 2 | ACTIVE_NOT_RECRUITING | NCT05261906 |
| Navitor Transcatheter Aortic Valve, FlexNav Delivery System, Navitor Loading System | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06008080 |
| Implanted with a Nanostim leadless pacemaker system | Other | Preclinical | Indications for VVI(R) Pacemaker | COMPLETED | NCT02051972 |
| JETi lower extremity arterial thrombosis | Other | Preclinical | Arterial Thrombosis | COMPLETED | NCT04370691 |
| CardioMEMS | Other | Approved | Heart Failure With Reduced Ejection Fraction | RECRUITING | NCT06241430 |
| CardioMEMS | Other | Approved | Heart Failure With Reduced Ejection Fraction | RECRUITING | NCT06241430 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Band | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Tailor Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Séguin Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Abbott SJM Rigid Saddle Ring | Other | Preclinical | Mitral Regurgitation | RECRUITING | NCT04761120 |
| Leadless Pacemaker | Other | Approved | Bradycardia | COMPLETED | NCT02030418 |
| Leadless Pacemaker | Other | Approved | Bradycardia | COMPLETED | NCT02030418 |
| MitraClip G4 System | Other | Preclinical | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04177394 |
| MitraClip G4 System | Other | Preclinical | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04177394 |
| MitraClip G4 System | Other | Preclinical | Mitral Valve Regurgitation | ACTIVE_NOT_RECRUITING | NCT04177394 |
| ICM Implantation | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| Standard of Care | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| ICM Implantation | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| Standard of Care | Other | Approved | Acute Myocardial Infarction | RECRUITING | NCT05073419 |
| Tendyne Mitral Valve System | Other | Approved | Mitral Valve Regurgitation | COMPLETED | NCT02321514 |
| Commercially available transcatheter aortic valve | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02000115 |
| Portico transcatheter aortic valve | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02000115 |
| Continuous Saline Thermodilution | Other | Preclinical | ST Elevation Myocardial Infarction | RECRUITING | NCT06795035 |
| Continuous Saline Thermodilution | Other | Preclinical | ST Elevation Myocardial Infarction | RECRUITING | NCT06795035 |
| Continuous Saline Thermodilution | Other | Preclinical | ST Elevation Myocardial Infarction | RECRUITING | NCT06795035 |
| Single-Chamber Transvenous Pacemaker | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05336877 |
| Aveir VR Leadless Pacemaker System | Other | Preclinical | Cardiac Pacemaker | RECRUITING | NCT05336877 |
| Navitor Titan Valve (35mm) Valve and Large FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Portico™ NG (Navitor) Valve and FlexNav™ Delivery System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04011722 |
| Calorie restriction via total food replacement | Other | Approved | Type 2 Diabetes | COMPLETED | NCT05754775 |
| Calorie restriction via total food replacement | Other | Approved | Type 2 Diabetes | COMPLETED | NCT05754775 |
| CardioMEMS™ HF System | Other | Approved | Heart Failure | COMPLETED | NCT03387813 |
| PressureWire Certus guidewire | Other | Approved | Multi Vessel Coronary Artery Disease | COMPLETED | NCT02325973 |
| The TriClip System | Other | Preclinical | Tricuspid Regurgitation | RECRUITING | NCT06920745 |
| The TriClip System | Other | Preclinical | Tricuspid Regurgitation | RECRUITING | NCT06920745 |
| Radiofrequency catheter ablation +EPS guided trigger and substrate ablation | Other | Approved | Atrial Fibrillation | NOT_YET_RECRUITING | NCT04823299 |
| Cryoballoon ablation | Other | Approved | Atrial Fibrillation | NOT_YET_RECRUITING | NCT04823299 |
| Radiofrequency catheter ablation +EPS guided trigger and substrate ablation | Other | Approved | Atrial Fibrillation | NOT_YET_RECRUITING | NCT04823299 |
| Cryoballoon ablation | Other | Approved | Atrial Fibrillation | NOT_YET_RECRUITING | NCT04823299 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Roll-over | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Upgrades | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Single-chamber atrial Aveir patients | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Aveir DR Leadless Pacemaker Implant | Other | Preclinical | Leadless Pacemaker | RECRUITING | NCT07106788 |
| Oral Nutritional Supplement (ONS) | Other | Preclinical | Malnutrition | COMPLETED | NCT05913193 |
| capillary blood glucose monitoring | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07157384 |
| Intermittently scanned continuous glucose monitoring | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07157384 |
| Diabetes self management education | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07157384 |
| Low calorie meal replacement plan | Other | Approved | Type 2 Diabetes | NOT_YET_RECRUITING | NCT07157384 |
| placebo | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT01385826 |
| Anti-tumor necrosis factor alpha monoclonal antibody | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT01385826 |
| placebo | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT01385826 |
| Anti-tumor necrosis factor alpha monoclonal antibody | Other | Phase PHASE2 | Uveitis | COMPLETED | NCT01385826 |
| Self-reported risk screening for PrEP and syndromic management for STIs | Other | Approved | Gonorrhea Female | RECRUITING | NCT06743204 |
| Self-Reported Risk Screening for PrEP and Diagnostic STI testing | Other | Approved | Gonorrhea Female | RECRUITING | NCT06743204 |
| Self-reported risk screening for PrEP and syndromic management for STIs | Other | Approved | Gonorrhea Female | RECRUITING | NCT06743204 |
| Self-Reported Risk Screening for PrEP and Diagnostic STI testing | Other | Approved | Gonorrhea Female | RECRUITING | NCT06743204 |
| Simethicone | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Mebeverine | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Mebeverine+Simethicone | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Simethicone | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Mebeverine | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Mebeverine+Simethicone | Other | Phase PHASE3 | Functional Bowel Disorder | COMPLETED | NCT05175131 |
| Peripheral PTA with a drug coated balloon | Drug | Approved | Femoral Artery Stenosis | COMPLETED | NCT05734157 |
| Drug Eluting Balloon | Drug | Approved | In-stent Restenosis | COMPLETED | NCT05731700 |
| Peripheral vascular flow reserve measurement | Other | Approved | Peripheral Arterial Disease | WITHDRAWN | NCT06014242 |
| Experimental Liquid Supplement | Other | Approved | Exercise Induced Muscle Damage | COMPLETED | NCT06205537 |
| Control Liquid Supplement | Other | Approved | Exercise Induced Muscle Damage | COMPLETED | NCT06205537 |
| Experimental Liquid Supplement | Other | Approved | Exercise Induced Muscle Damage | COMPLETED | NCT06205537 |
| Control Liquid Supplement | Other | Approved | Exercise Induced Muscle Damage | COMPLETED | NCT06205537 |
| Placing a guidewire in Coronary sinus for measurement of Q-LV during His Bundle pacing or, if needed, for LV pacing | Other | Approved | Heart Failure | COMPLETED | NCT03803995 |
| Mapping and Pacing the His Bundle | Other | Approved | Heart Failure | COMPLETED | NCT03803995 |
| Placing a guidewire in Coronary sinus for measurement of Q-LV during His Bundle pacing or, if needed, for LV pacing | Other | Approved | Heart Failure | COMPLETED | NCT03803995 |
| Mapping and Pacing the His Bundle | Other | Approved | Heart Failure | COMPLETED | NCT03803995 |
| MuscleSCS | Other | Approved | Chronic Low Back Pain (CLBP) | RECRUITING | NCT07215104 |
| Any Commercially Available Transcatheter Aortic Valve (CAV) System | Other | Approved | Aortic Valve Stenosis | ENROLLING_BY_INVITATION | NCT05932615 |
| Navitor Transcatheter Aortic Valve Implantation (TAVI) System | Other | Approved | Aortic Valve Stenosis | ENROLLING_BY_INVITATION | NCT05932615 |
| Pulsed Field Ablation | Other | Approved | Atrial Arrhythmia | RECRUITING | NCT06106594 |
| FlexAbility SE Ablation Catheter | Other | Preclinical | Ventricular Tachycardia | ACTIVE_NOT_RECRUITING | NCT05839873 |
| Dorsal Root Ganglion Stimulation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05103527 |
| Dorsal Root Ganglion Stimulation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05103527 |
| Dorsal Root Ganglion Stimulation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05103527 |
| Abbott Mechanical Heart Valve (MHV) Regent™ | Other | Preclinical | Valvular Heart Disease | COMPLETED | NCT05330468 |
| Ensure Surgery Immunonutrition shake | Procedure | Approved | Heart Failure | RECRUITING | NCT05655910 |
| POC BG + Blinded CGM | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07045298 |
| Libre 2 rt-CGM | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07045298 |
| Conventional | Other | Approved | Percutaneous Coronary Intervention | COMPLETED | NCT04253171 |
| Lithoplasty | Other | Approved | Percutaneous Coronary Intervention | COMPLETED | NCT04253171 |
| Conventional | Other | Approved | Percutaneous Coronary Intervention | COMPLETED | NCT04253171 |
| Lithoplasty | Other | Approved | Percutaneous Coronary Intervention | COMPLETED | NCT04253171 |
| mFOLFOX-6 | Other | Phase PHASE1 | Metastatic Pancreatic Cancer | COMPLETED | NCT01489865 |
| ABT-888 | Other | Phase PHASE1 | Metastatic Pancreatic Cancer | COMPLETED | NCT01489865 |
| mFOLFOX-6 | Other | Phase PHASE1 | Metastatic Pancreatic Cancer | COMPLETED | NCT01489865 |
| ABT-888 | Other | Phase PHASE1 | Metastatic Pancreatic Cancer | COMPLETED | NCT01489865 |
| electrophysiology study and ablation with an Abbott Ablation Catheter | Other | Preclinical | Atrial Arrhythmia | ACTIVE_NOT_RECRUITING | NCT05434650 |
| Navitor Transcatheter Aortic Valve Implantation | Other | Preclinical | Severe Aortic Stenosis | RECRUITING | NCT07193888 |
| BurstDR Spinal Cord Stimulation | Other | Approved | Painful Diabetic Neuropathy (PDN) | ENROLLING_BY_INVITATION | NCT07250828 |
| cardiac surgery | Procedure | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03271762 |
| percutaneous mitral valve repair with MITRACLIP NT, MITRACLIP NTR/XTR, MITRACLIP G4NT/XT, MITRACLIP G4NTW/XTW | Other | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03271762 |
| GnRH antagonist protocol | Other | Approved | Diminished Ovarian Reserve | RECRUITING | NCT05847283 |
| Dydrogesterone priming ovarian stiumulation protocol | Other | Approved | Diminished Ovarian Reserve | RECRUITING | NCT05847283 |
| Biomarker Testing using the Alinity Whole-blood TBI biomarker i-STAT | Other | Approved | Brain Injuries | RECRUITING | NCT06932588 |
| Biomarker Testing using the Alinity Whole-blood TBI biomarker i-STAT | Other | Approved | Brain Injuries | RECRUITING | NCT06932588 |
| MitraClip procedure | Procedure | Approved | Mitral Regurgitation | COMPLETED | NCT04259411 |
| JETi Hydrodynamic Thrombectomy System | Other | Preclinical | Peripheral Venous Thrombosis | COMPLETED | NCT06340763 |
| HeartMate 3 (R) left ventricular assist device | Device | Preclinical | LVAD | RECRUITING | NCT06039176 |
| HeartMate 3 (R) left ventricular assist device | Device | Preclinical | LVAD | RECRUITING | NCT06039176 |
| HeartMate 3 (R) left ventricular assist device | Device | Preclinical | LVAD | RECRUITING | NCT06039176 |
| Blood draw | Other | Approved | Hematologic Tests | RECRUITING | NCT07287618 |
| OCT-guided PCI | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Extended DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Standard DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Short DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| OCT-guided PCI | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Extended DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Standard DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Short DAPT | Other | Approved | Stable Angina | RECRUITING | NCT07198529 |
| Left Atrial Appendage (LAA) closure procedure with Amplatzer Amulet LAA occluder | Procedure | Preclinical | Non-Valvular Atrial Fibrillation | TERMINATED | NCT06189365 |
| Coroventis Coroflow Cardiovascular System and PressureWire™ X Guidewire | Other | Preclinical | Ischemia and No Obstructive Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05288361 |
| Coroventis Coroflow Cardiovascular System and PressureWire™ X Guidewire | Other | Preclinical | Ischemia and No Obstructive Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05288361 |
| Fixed AV delay | Other | Approved | Congestive Heart Failure | ACTIVE_NOT_RECRUITING | NCT04100148 |
| SyncAV programmed ON | Other | Approved | Congestive Heart Failure | ACTIVE_NOT_RECRUITING | NCT04100148 |
| Confirm Rx ICM insertion procedure | Procedure | Preclinical | Cardiac Arrhythmias | ACTIVE_NOT_RECRUITING | NCT03505801 |
| Libre 3 continuous glucose monitoring sensor | Other | Preclinical | Gestational Diabetes | ACTIVE_NOT_RECRUITING | NCT05981547 |
| Libre 3 continuous glucose monitoring sensor | Other | Preclinical | Gestational Diabetes | ACTIVE_NOT_RECRUITING | NCT05981547 |
| femoropopliteal revascularization for TASC C or TASC D lesion | Other | Approved | Superficial Femoral Artery Stenosis | RECRUITING | NCT04434586 |
| femoropopliteal revascularization for TASC C or TASC D lesion | Other | Approved | Superficial Femoral Artery Stenosis | RECRUITING | NCT04434586 |
| XIENCE Xpedition/Alpine/Sierra | Other | Preclinical | Percutaneous Transluminal Coronary Angioplasty | COMPLETED | NCT02042300 |
| Esprit BTK™ Everolimus Eluting Resorbable Scaffold from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270575 |
| Esprit BTK™ Everolimus Eluting Resorbable Scaffold from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270575 |
| Percutaneous Transluminal Angioplasty (PTA) Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT04227899 |
| Esprit BTK Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT04227899 |
| Percutaneous Transluminal Angioplasty (PTA) Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT04227899 |
| Esprit BTK Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT04227899 |
| Stealth 360™ Peripheral Orbital Atherectomy System from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270562 |
| Stealth 360™ Peripheral Orbital Atherectomy System from Abbott | Other | Preclinical | Chronic Limb Threatening Ischemia | NOT_YET_RECRUITING | NCT07270562 |
| Optical coherence tomography measurements | Other | Preclinical | Femoropopliteal Stenosis | ACTIVE_NOT_RECRUITING | NCT05057637 |
| Optical coherence tomography measurements | Other | Preclinical | Femoropopliteal Stenosis | ACTIVE_NOT_RECRUITING | NCT05057637 |
| Optical coherence tomography measurements | Other | Preclinical | Femoropopliteal Stenosis | ACTIVE_NOT_RECRUITING | NCT05057637 |
| Dorsal root ganglion stimulation (DRG) | Other | Preclinical | Chronic Pain | RECRUITING | NCT03876054 |
| Spinal cord stimulation (SCS) | Other | Preclinical | Chronic Pain | RECRUITING | NCT03876054 |
| Deep Brain Stimulation (DBS) | Other | Preclinical | Movement Disorders | RECRUITING | NCT04071847 |
| Oral itraconazole 200mg daily for 5 days | Other | Phase PHASE1 | Pityriasis Versicolor | NOT_YET_RECRUITING | NCT07331792 |
| Topical 1 % clotrimazole twice daily 2 weeks | Other | Phase PHASE1 | Pityriasis Versicolor | NOT_YET_RECRUITING | NCT07331792 |
| Oral itraconazole 200mg daily for 5 days | Other | Phase PHASE1 | Pityriasis Versicolor | NOT_YET_RECRUITING | NCT07331792 |
| Topical 1 % clotrimazole twice daily 2 weeks | Other | Phase PHASE1 | Pityriasis Versicolor | NOT_YET_RECRUITING | NCT07331792 |
| DBS of the NAc | Other | Approved | Opioid-use Disorder | RECRUITING | NCT04354077 |
| DBS of the NAc | Other | Approved | Opioid-use Disorder | RECRUITING | NCT04354077 |
| Automated closed-loop insulin delivery | Other | Approved | Diabete Type 1 | RECRUITING | NCT07240012 |
| Automated closed-loop insulin delivery | Other | Approved | Diabete Type 1 | RECRUITING | NCT07240012 |
| PFA Ablation catheter | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT06676072 |
| Esprit BTK Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT05208905 |
| Esprit BTK Device | Device | Approved | Critical Limb Ischemia (CLI) | ACTIVE_NOT_RECRUITING | NCT05208905 |
| FFR>0.80+ OCT with findings indicative of vulnerable plaque | Other | Approved | Coronary Artery Disease | RECRUITING | NCT05599061 |
| FFR>0.80+ OCT with findings indicative of vulnerable plaque | Other | Approved | Coronary Artery Disease | RECRUITING | NCT05599061 |
| protein supplement | Other | Approved | Type 2 Diabetes | RECRUITING | NCT07271043 |
| protein supplement | Other | Approved | Type 2 Diabetes | RECRUITING | NCT07271043 |
| Blood draw | Other | Preclinical | Activated Clotting Time | ACTIVE_NOT_RECRUITING | NCT07382076 |
| Blood draw | Other | Preclinical | Activated Clotting Time | ACTIVE_NOT_RECRUITING | NCT07382076 |
| TactiFlex™ Ablation Catheter Sensor Enabled™ | Other | Approved | Atrial Fibrillation Paroxysmal | COMPLETED | NCT06271967 |
| Cephea Mitral Valve System | Other | Approved | Mitral Regurgitation | RECRUITING | NCT07244939 |
| Abbott BE TAVI System | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT07116551 |
| Percutaneous coronary intervention | Other | Preclinical | Acute Coronary Syndrome | COMPLETED | NCT04475380 |
| AVP III | Other | Approved | Paravalvular Aortic Regurgitation | ACTIVE_NOT_RECRUITING | NCT04489823 |
| Non-Vitamin K Oral Antagonists | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04226547 |
| Left Atrial Appendage Occlusion (Amplatzer Amulet LAA Occluder) | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04226547 |
| Non-Vitamin K Oral Antagonists | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04226547 |
| Left Atrial Appendage Occlusion (Amplatzer Amulet LAA Occluder) | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04226547 |
| Guideline Medical Directed Therapy | Drug | Approved | Heart Failure | RECRUITING | NCT06526195 |
| HeartMate 3 Left Ventricular Assist System | Other | Approved | Heart Failure | RECRUITING | NCT06526195 |
| CardioMEMS HF System | Other | Approved | Heart Failure | RECRUITING | NCT06526195 |
| Amulet™ 2 Left Atrial Appendage (LAA) Occluder | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT06707688 |
| Amulet™ 2 Left Atrial Appendage (LAA) Occluder | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT06707688 |
| MULTI-DOMAIN LIFESTILE INTERVENTION | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT06025994 |
| Placebo | Other | Phase PHASE4 | Hepatitis B | COMPLETED | NCT05705427 |
| Hepatitis B monovalent vaccine | Other | Phase PHASE4 | Hepatitis B | COMPLETED | NCT05705427 |
| Tenofovir Disoproxil Fumarate 300 MG | Other | Phase PHASE4 | Hepatitis B | COMPLETED | NCT05705427 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| XIENCE Skypoint Large Vessel Everolimus Eluting Coronary Stent System (EECSS) | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05423379 |
| Amplatzer Amulet Left Atrial Appendage Occlusion Device | Device | Preclinical | Atrial Fibrillation | COMPLETED | NCT05687591 |
| Atrial Fibrillation Radiofrequency Ablation Only | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| catheter ablation combined with LAAO (Left Atrial Appendage Occlusion) | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| Atrial Fibrillation Radiofrequency Ablation Only | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| catheter ablation combined with LAAO (Left Atrial Appendage Occlusion) | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| Atrial Fibrillation Radiofrequency Ablation Only | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| catheter ablation combined with LAAO (Left Atrial Appendage Occlusion) | Other | Approved | Atrial Fibrillation (AF) | NOT_YET_RECRUITING | NCT07441382 |
| Continuous Glucose Monitoring (CGM) | Other | Approved | Diabetes | NOT_YET_RECRUITING | NCT07135531 |
| Continuous Glucose Monitoring (CGM) | Other | Approved | Diabetes | NOT_YET_RECRUITING | NCT07135531 |
| Investigational Reflex Test 3 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 2 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 1 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 3 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 2 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 1 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 3 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 2 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Investigational Reflex Test 1 | Other | Preclinical | Neisseria Gonorrheae Infection | RECRUITING | NCT06815536 |
| Standard of Care (SOC) | Other | Approved | Diabetes | ACTIVE_NOT_RECRUITING | NCT06632002 |
| DSF2 | Other | Approved | Diabetes | ACTIVE_NOT_RECRUITING | NCT06632002 |
| DSF1 | Other | Approved | Diabetes | ACTIVE_NOT_RECRUITING | NCT06632002 |
| Transseptal procedure with Agilis RF TSP System. | Procedure | Approved | Cardiac Arrythmias | RECRUITING | NCT07361445 |
| AMPLATZER™ PFO Occluder | Other | Approved | Stroke | ACTIVE_NOT_RECRUITING | NCT03309332 |
| Standard of Care | Other | Preclinical | Cardiac Rhythm Disorder | COMPLETED | NCT04460209 |
| MitraClip System | Other | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03433274 |
| Tendyne Mitral Valve System | Other | Approved | Mitral Regurgitation | ACTIVE_NOT_RECRUITING | NCT03433274 |
| (ELEVATE-AF X) control group | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT06883864 |
| (ELEVATE-AF X) experimental group | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT06883864 |
| Medication | Drug | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT06883864 |
| Catheter ablation plus medication | Drug | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT06883864 |
| Stratification and standard care | Other | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| Stratified medicine - Microvascular dysfunction and eplerenone therapy, tablets | Drug | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| Stratification and standard care | Other | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| Stratified medicine - Microvascular dysfunction and eplerenone therapy, tablets | Drug | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| Stratification and standard care | Other | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| Stratified medicine - Microvascular dysfunction and eplerenone therapy, tablets | Drug | Phase PHASE2 | Myocardial Infarction, Acute | RECRUITING | NCT05198791 |
| CardioMEMS implantation with routine ambulatory pulmonary artery pressure monitoring and medication optimization | Drug | Approved | Cardiogenic Shock | RECRUITING | NCT04419480 |
| CardioMEMS implantation with routine ambulatory pulmonary artery pressure monitoring and medication optimization | Drug | Approved | Cardiogenic Shock | RECRUITING | NCT04419480 |
| CardioMEMS implantation with routine ambulatory pulmonary artery pressure monitoring and medication optimization | Drug | Approved | Cardiogenic Shock | RECRUITING | NCT04419480 |
| LBBAP Implant with a CSP ICD Lead | Other | Approved | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06830746 |
| ViewFlex X ICE System | Other | Preclinical | Cardiac Arrhythmias | RECRUITING | NCT06772493 |
| ViewFlex X ICE System | Other | Preclinical | Cardiac Arrhythmias | RECRUITING | NCT06772493 |
| Conventional Management and monitoring | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| ASSERT Insertable Cardiac Monitor | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| Conventional Management and monitoring | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| ASSERT Insertable Cardiac Monitor | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| Conventional Management and monitoring | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| ASSERT Insertable Cardiac Monitor | Other | Approved | Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT04818645 |
| Antiplatelet therapy | Drug | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Oral Anticoagulant, Direct-Acting | Other | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Transcatheter PFO closure | Other | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Antiplatelet therapy | Drug | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Oral Anticoagulant, Direct-Acting | Other | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Transcatheter PFO closure | Other | Phase PHASE3 | Cryptogenic Ischemic Stroke | RECRUITING | NCT05387954 |
| Esprit BTK System | Other | Approved | Chronic Limb-Threatening Ischemia | ACTIVE_NOT_RECRUITING | NCT06656364 |
| AVEIR CSP Leadless Pacemaker System | Other | Approved | Cardiac Pacemaker | ACTIVE_NOT_RECRUITING | NCT07287423 |
| No intervention planned | Other | Preclinical | Myocardial Ischemia | ACTIVE_NOT_RECRUITING | NCT05324683 |
| No intervention planned | Other | Preclinical | Myocardial Ischemia | ACTIVE_NOT_RECRUITING | NCT05324683 |
| The TriClip System | Other | Preclinical | Tricuspid Regurgitation | RECRUITING | NCT07509658 |
| CardioMEMS HF System | Other | Preclinical | Heart Failure | RECRUITING | NCT06779552 |
| CardioMEMS HF System | Other | Preclinical | Heart Failure | RECRUITING | NCT06779552 |
| Itopride Hydrochloride 50 mg film coated tablets | Other | Phase PHASE3 | Functional Dyspepsia | COMPLETED | NCT06217393 |
| Itopride Hydrochloride 150 mg extended release tablets | Other | Phase PHASE3 | Functional Dyspepsia | COMPLETED | NCT06217393 |
| Itopride Hydrochloride 50 mg film coated tablets | Other | Phase PHASE3 | Functional Dyspepsia | COMPLETED | NCT06217393 |
| Itopride Hydrochloride 150 mg extended release tablets | Other | Phase PHASE3 | Functional Dyspepsia | COMPLETED | NCT06217393 |
| AMJ-401 | Other | Approved | Ischemic Heart Disease (IHD) | RECRUITING | NCT07373353 |
| AMJ-401 | Other | Approved | Ischemic Heart Disease (IHD) | RECRUITING | NCT07373353 |
| Kaletra (lopinavir/ritonavir) + Combivir (zidovudine/lamivudine) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00424814 |
| Kaletra (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00424814 |
| Kaletra (lopinavir/ritonavir) + Combivir (zidovudine/lamivudine) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00424814 |
| Kaletra (lopinavir/ritonavir) | Other | Phase PHASE2 | HIV Infections | COMPLETED | NCT00424814 |
| Balloon expandable TAVI | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT07082426 |
| Cephea Mitral Valve System | Other | Approved | Mitral Regurgitation | RECRUITING | NCT05061004 |
| Veliparib | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Pharmacological Study | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Paclitaxel | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Carboplatin | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| FreeStyle Libre 3 | Other | Preclinical | Pre Diabetes | RECRUITING | NCT06921902 |
| Experimental | Other | Approved | Coronary Artery Calcification | RECRUITING | NCT06885177 |
| FreeStyle Libre 2 | Other | Preclinical | Diabete Mellitus | ACTIVE_NOT_RECRUITING | NCT04959552 |
| Experimental Nutrition Product | Other | Approved | Gastrointestinal Tolerance | RECRUITING | NCT07426406 |
| Behavioral Treatment, Speech Therapy | Drug | Approved | Autism Spectrum Disorder (ASD | ACTIVE_NOT_RECRUITING | NCT06733324 |
| SCERTS (Social Communication, Emotional Regulation, Transactional Support) | Other | Approved | Autism Spectrum Disorder (ASD | ACTIVE_NOT_RECRUITING | NCT06733324 |
| Behavioral Treatment, Speech Therapy | Drug | Approved | Autism Spectrum Disorder (ASD | ACTIVE_NOT_RECRUITING | NCT06733324 |
| SCERTS (Social Communication, Emotional Regulation, Transactional Support) | Other | Approved | Autism Spectrum Disorder (ASD | ACTIVE_NOT_RECRUITING | NCT06733324 |
| Epic™ Surgical Tissue Heart Valve devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Amplatzer™ Occlusion Devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Epic™ Surgical Tissue Heart Valve devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Amplatzer™ Occlusion Devices | Device | Preclinical | Heart Diseases | RECRUITING | NCT06590467 |
| Navitor Transcatheter Aortic valve and FlexNav Delivery system | Other | Approved | Symptomatic Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04788888 |
| CAVGJ | Other | Preclinical | Aortic Valve Disease | RECRUITING | NCT04754217 |
| VAVGJ | Other | Preclinical | Aortic Valve Disease | RECRUITING | NCT04754217 |
| Aortic Valve Replacement | Other | Preclinical | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT03924661 |
| Aortic Valve Replacement | Other | Preclinical | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT03924661 |
| Veliparib | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Pharmacological Study | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Paclitaxel | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Carboplatin | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Veliparib | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Pharmacological Study | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Paclitaxel | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Carboplatin | Other | Phase PHASE1 | Breast Carcinoma | ACTIVE_NOT_RECRUITING | NCT01366144 |
| Active-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Sham-stimulation | Other | Approved | Treatment Resistant Depression | RECRUITING | NCT06423430 |
| Grid X and EnSite X v3.1.1 Software | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | RECRUITING | NCT07421076 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| OCT Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| Angiographic Guided PCI | Other | Approved | Ischemic Heart Disease | ENROLLING_BY_INVITATION | NCT07422688 |
| LBBAP lead | Other | Approved | Bradycardia | RECRUITING | NCT07217392 |
| Intravascular imaging (OCT), Invasive physiologic assessment (FFR, CFR, IMR), or Non-invasive physiologic assessment (N-13 ammonia PET) | Other | Preclinical | Myocardial Infarction | RECRUITING | NCT05272618 |