- Trials with a EudraCT protocol (436)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
436 result(s) found for: Fibrillation.
Displaying page 4 of 22.
EudraCT Number: 2004-000359-41 | Sponsor Protocol Number: D1250C00007 | Start Date*: 2004-08-31 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Controlled, Randomised, Parallel, Multicentre Study to Assess Safety and Tolerability of the Oral Direct Thrombin Inhibitor AZD0837 in the Prevention of Stroke and other Thromboembolic Complicati... | |||||||||||||
Medical condition: Prevention of stroke and other thromboembolic complications associated with Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004399-68 | Sponsor Protocol Number: 1925-201-008 | Start Date*: 2019-03-29 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Dose Ranging Study to Evaluate the Efficacy and Safety of Botulinum Toxin Type A (AGN 151607) Injections into the Epicardial F... | |||||||||||||
Medical condition: Post-operative atrial fibrillation (POAF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) AT (Completed) SE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002789-18 | Sponsor Protocol Number: RAF-01 | Start Date*: 2011-11-15 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND, DOUBLE-DUMMY, PLACEBO-CONTROLLED, DOSE-RANGING PHASE II STUDY ASSESSING RANOLAZINE IN THE MAINTENANCE OF SINUS RHYTHM AFTER ELECTRICAL CARDIOVERSION IN PATIENTS WITH NON... | |||||||||||||
Medical condition: NON-PERMANENT ATRIAL FIBRILLATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002234-39 | Sponsor Protocol Number: BAY59-7939/15693 | Start Date*: 2012-08-07 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A prospective, randomized, open-label, parallel-group, active-controlled, multicenter study exploring the efficacy and safety of once-daily oral rivaroxaban (BAY 59-7939) compared with that of dose... | |||||||||||||
Medical condition: prevention of stroke and non-central nervous system systemic embolism in subjects with non-valvular atrial fibrillation scheduled for cardioversion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) PT (Completed) ES (Completed) NL (Completed) DE (Completed) GR (Completed) BE (Completed) GB (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005625-29 | Sponsor Protocol Number: VERI-305-AMIO | Start Date*: 2008-03-06 | |||||||||||
Sponsor Name:Cardiome Pharma Corp. | |||||||||||||
Full Title: A Phase III Prospective, Randomized, Double-Blind, Active-Controlled, Multi-Center, Superiority Study of Vernakalant Injection versus Amiodarone in Subjects with Recent Onset Atrial Fibrillation | |||||||||||||
Medical condition: Treatment of Atrial fibrillation (AF). AF is the most common arrhythmia encountered in clinical practice. It is usually associated with age and general physical condition, rather than with a speci... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) FR (Completed) LT (Completed) EE (Completed) DK (Completed) CZ (Completed) FI (Completed) SK (Completed) LV (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005246-20 | Sponsor Protocol Number: 142 | Start Date*: 2008-03-11 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital, Skejby | ||||||||||||||||||
Full Title: Amiodarone prophylaxis for atrial fibrillation in patients undergoing surgery for lung cancer: A controlled, randomized, double blinded trial. | ||||||||||||||||||
Medical condition: Atrial fibrillation after lung resection due to cancer in the lung | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005503-84 | Sponsor Protocol Number: AFNET8 | Start Date*: 2018-02-14 | ||||||||||||||||
Sponsor Name:Kompetenznetz Vorhofflimmern e.V. | ||||||||||||||||||
Full Title: A Safety Study Assessing Oral Anticoagulation with Apixaban versus Vitamin-K Antagonists in Patients with Atrial Fibrillation and End-Stage Kidney Disease (ESKD) on Chronic Hemodialysis Treatment. | ||||||||||||||||||
Medical condition: End-Stage Kidney Disease (ESKD) on Chronic Hemodialysis Treatment and Atrial Fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005022-18 | Sponsor Protocol Number: PACeS | Start Date*: 2022-07-26 | |||||||||||
Sponsor Name:Icahn School of Medicine at Mount Sinai | |||||||||||||
Full Title: Anticoagulation for New-Onset Post-Operative Atrial Fibrillation after CABG | |||||||||||||
Medical condition: New-Onset Post-Operative Atrial Fibrillation after CABG | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005043-13 | Sponsor Protocol Number: RG_14-187 | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Evaluating different rate control therapies in permanent atrial fibrillation: A prospective, randomised, open-label, blinded endpoint study comparing digoxin and beta-blockers as initial rate contr... | |||||||||||||
Medical condition: Atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003619-30 | Sponsor Protocol Number: BAY 68-4986/12679 | Start Date*: 2007-12-27 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Study to investigate the effect of the A1 agonist capadenoson on ventricular HR in patients with persistent or permanent atrial fibrillation by administration of capadenoson in a dose of 4 mg once ... | |||||||||||||
Medical condition: Atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003702-33 | Sponsor Protocol Number: RG_14-150 | Start Date*: 2015-01-23 | |||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||
Full Title: IMPRESS-AF: IMproved exercise tolerance in patients with PReserved Ejection fraction by Spironolactone on myocardial fibrosiS in Atrial Fibrillation | |||||||||||||||||||||||
Medical condition: Atrial fibrillation with preserved left ventricular systolic function and normal levels of the brain natriuretic peptide. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003100-13 | Sponsor Protocol Number: KKSH-154 | Start Date*: 2020-08-03 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Pharmacokinetics of edoxaban in patients with advanced chronic kidney disease (CKD) treated for stroke prevention | |||||||||||||
Medical condition: Nonvalvular Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000058-21 | Sponsor Protocol Number: CLOSURE-AF-DZHK16 | Start Date*: 2018-03-01 | |||||||||||
Sponsor Name:Charité – Universitätsmedizin Berlin, Campus Benjamin Franklin | |||||||||||||
Full Title: Left atrial appendage CLOSURE in patients with Atrial Fibrillation at high risk of stroke and bleeding compared to medical therapy: a prospective randomized clinical trial | |||||||||||||
Medical condition: Atrial Fibrillation with high risk of stroke and bleeding | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003890-40 | Sponsor Protocol Number: 1160.204 | Start Date*: 2015-02-24 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim Italia S.p.A. | ||||||||||||||||||
Full Title: Randomized Evaluation of dabigatran etexilate Compared to warfarIn in pulmonaRy vein ablation: assessment of an uninterrupted periproCedUral alntIcoagulation sTrategy (The RE-CIRCUIT Trial) | ||||||||||||||||||
Medical condition: Patients with non-valvular atrial fibrillation (NVAF) undergoing catheter ablation for atrial fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) ES (Completed) NL (Completed) DE (Completed) BE (Completed) GB (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001430-18 | Sponsor Protocol Number: 5101127 | Start Date*: 2019-08-12 |
Sponsor Name:Kuopio University Hospital | ||
Full Title: Does postoperative intravenous corticosteroid and intravenous beta blocker management prevent atrial fibrillation after cardiac surgery? | ||
Medical condition: new onset atrial fibrillation and paroxysmal atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005525-48 | Sponsor Protocol Number: AK-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Diakonhjemmet hospital | ||
Full Title: Potassium infusion for conversion of atrial fibrillation/atrial flutter. | ||
Medical condition: Atrial fibrillation / atrial flutter | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001491-11 | Sponsor Protocol Number: RIVAROXAFL3003 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: An OPen-label, Randomized, Controlled, Multicenter Study ExplorIng TwO TreatmeNt StratEgiEs of Rivaroxaban and a Dose-Adjusted Oral Vitamin K Antagonist Treatment Strategy in Subjects With Atrial ... | |||||||||||||
Medical condition: Prevention of stroke and non-CNS systemic embolism in patients with nonvalvular atrial fibrillation who undergo percutaneous coronary intervention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) SE (Completed) IT (Completed) NL (Completed) DK (Completed) PL (Completed) BG (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002338-35 | Sponsor Protocol Number: 144 | Start Date*: 2013-05-06 | |||||||||||
Sponsor Name:Biosense Webster, Inc. | |||||||||||||
Full Title: ATrial FibrillaTion ProgrESsion Trial (ATTEST Trial) | |||||||||||||
Medical condition: Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) ES (Completed) IE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001795-30 | Sponsor Protocol Number: DU176b-C-E314 | Start Date*: 2016-11-11 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: Evaluation of Edoxaban in Anticoagulant Naïve Patients with Non-Valvular Atrial Fibrillation (NVAF) and high Creatinine Clearance | |||||||||||||
Medical condition: Non-Valvular Atrial Fibrillation (NVAF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) CZ (Completed) EE (Completed) LT (Completed) SK (Completed) DK (Completed) HU (Completed) ES (Completed) BE (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005977-37 | Sponsor Protocol Number: 08-015 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Portola Pharmaceuticals Inc. | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, PARALLEL GROUP, DOSE-FINDING, MULTICENTER, MULTINATIONAL STUDY OF THE SAFETY, TOLERABILITY AND PILOT EFFICACY OF THREE BLINDED DOSES OF THE ORAL FACTOR Xa INHIBITOR BETRIXABA... | |||||||||||||
Medical condition: Antithrombotic treatment for prevention of stroke in patients with non-valvular atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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