Found 32 matching trials
Japanese Pradaxa PMS, Long Term N/A The study objective is to confirm appropriate use and safety profile of Pra...
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Nippon Boehringer Ingelheim Co., Ltd
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Left Atrial Appendage CLOSURE in Patients With Atrial Fibrillation Compared to Medical Therapy PHASE4 The study goal is to determine the clinical benefit of percutaneous cathete...
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Charité Universitätsmedizin Berlin, Klinik für Kardiologie, Angiologie und Intensivmedizin, Deutsches Herzzentrum der Charité, Campus Benjamin Franklin (CBF)
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Bioavailability of BIBR 1048 MS Single Doses With or Without Pantoprazole in Healthy Subjects PHASE1 The pharmacokinetics of 50 mg BIBR 1048 administered as two newly developed...
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Multiple Locations
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Bioequivalence Study of Dabigatran Etexilate Capsules 150 mg in Healthy Thai Volunteers Under Fasting Conditions PHASE1 The bioequivalence of Dabigatran Etexilate Capsules 150 mg to Boehringer In...
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Multiple Locations
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Reversal of Dabigatran With Prothrombin Complex Concentrate PHASE2 The purpose of this study is to investigate whether Prothrombin Complex Con...
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University Medical Centre
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Pioneering Advancements in Cardiocerebrovascular Interactions in the Asia pacFIC - Patent Foramen Ovale Study N/A A registry of patients from the Asia-Pacific region with PFO and ischemic s...
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National University Hospital
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AtriClip® Left Atrial Appendage Exclusion Concomitant to Structural Heart Procedures (ATLAS) PHASE4 Patients without a documented history of Atrial Fibrillation (AF) and will ...
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Sharp Memorial Hospital
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Clinical Trial for Optimal Novel Oral Anticoagulant (NOAC) Schedule Immediate Before Catheter Ablation for Atrial Fibrillation NA This study is to evaluated the interruption schedule of NOAC in patients wh...
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Severance Cardiovascular Hospital, Yonsei University Health System
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Resolution of Left Atrial-Appendage Thrombus - Effects of Dabigatran in Patients With AF PHASE2 The primary objective of this study is to assess whether Dabigatran leads t...
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University Heart Center; Department of Cardiology and Angiology II
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A Single Dose Bioequivalence Study of WD-1602 Versus Pradaxa® in Healthy Subjects Under Fed Condition PHASE1 This study will be a single-center, randomized, single-dose, open-label, tw...
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Multiple Locations
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