- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: CHA2DS2-VASc score.
Displaying page 1 of 2.
EudraCT Number: 2022-000758-28 | Sponsor Protocol Number: 19767 | Start Date*: 2022-11-23 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A multicenter, international, randomized, active comparator-controlled, double-blind, double-dummy, parallel-group, 2-arm, Phase 3 study to compare the efficacy and safety of the oral FXIa inhibito... | |||||||||||||||||||||||
Medical condition: Prevention of stroke or systemic embolism in atrial fibrillation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) DE (Trial now transitioned) BE (Trial now transitioned) FI (Trial now transitioned) AT (Trial now transitioned) ES (Trial now transitioned) SE (Trial now transitioned) HU (Trial now transitioned) NO (Trial now transitioned) SK (Trial now transitioned) LT (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) LV (Trial now transitioned) PT (Trial now transitioned) PL (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002365-35 | Sponsor Protocol Number: 19765 | Start Date*: 2020-01-24 | ||||||||||||||||
Sponsor Name:Bayer AG | ||||||||||||||||||
Full Title: Multicenter, randomized, active comparator-controlled, double-blind, double-dummy, parallel group, dose-finding Phase 2 study to compare the safety of the oral FXIa inhibitor BAY 2433334 to apixaba... | ||||||||||||||||||
Medical condition: Atrial Fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) SE (Completed) NL (Completed) FR (Completed) GB (GB - no longer in EU/EEA) HU (Completed) BE (Completed) LV (Completed) AT (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001013-32 | Sponsor Protocol Number: CV-185-685 | Start Date*: 2018-11-08 |
Sponsor Name:HOSPITAL CLÍNIC BARCELONA | ||
Full Title: ANTITHROMBOTIC THERAPY AFTER LEFT ATRIAL APPENDAGE OCCLUSION: DOUBLE ANTIPLATELET THERAPY VS. APIXABAN | ||
Medical condition: ATRIAL FIBRILLATION IN PATIENTS AFTER OCCLUSION OF THE LEFT ATRIAL APPENDAGE (LAAC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002075-33 | Sponsor Protocol Number: ENRICH-AF | Start Date*: 2020-05-05 | ||||||||||||||||
Sponsor Name:Hamilton Health Sciences, through its Population Health Research Institute | ||||||||||||||||||
Full Title: Edoxaban for intracranial hemorrhage survivors with atrial fibrillation | ||||||||||||||||||
Medical condition: High risk atrial fibrillation patients with previous intracranial hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NO (Prematurely Ended) DE (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) SK (Trial now transitioned) DK (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000721-11 | Sponsor Protocol Number: CHPAU2019/03 | Start Date*: 2020-09-24 | ||||||||||||||||
Sponsor Name:Centre hospitalier de PAU | ||||||||||||||||||
Full Title: Management of Anticoagulant Therapy monitored by an implantable device with telecardiology in patients with Acute Coronary Syndrome associated with de novo atrial Fibrillation Arrhythmia (SCA-FA): ... | ||||||||||||||||||
Medical condition: acute coronary syndrome and atrial fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000503-40 | Sponsor Protocol Number: GE IDE No. A01611 | Start Date*: 2011-04-12 | |||||||||||
Sponsor Name:Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen | |||||||||||||
Full Title: DABI-ADP-1: IMPACT OF DABIGATRAN AND PHENPROCOUMON ON ADP INDUCED PLATELET AGGREGATION IN PATIENTS WITH ATRIAL FIBRILLATION | |||||||||||||
Medical condition: Patients with atrial fibrillation and an indication for oral anticoagulation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005364-26 | Sponsor Protocol Number: RE-LATED-AF | Start Date*: 2014-07-17 |
Sponsor Name:University Medical Center of the Johannes Gutenberg University Mainz | ||
Full Title: Resolution of Left Atrial-Appendage Thrombus – Effects of Dabigatran in patients with AF (RE-LATED AF) – A Prospective, multicenter, randomized, open-label, controlled, explorative, blinded-endpoin... | ||
Medical condition: Left atrial-appendage thrombus in atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-005109-19 | Sponsor Protocol Number: ATTICUS | Start Date*: 2015-11-10 |
Sponsor Name:University Hospital Tuebingen | ||
Full Title: Apixaban for treatment of embolic stroke of undetermined source | ||
Medical condition: Patients with embolic stroke of undetermined source and at least on risk factor for cardiac embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-002741-29 | Sponsor Protocol Number: CMAA868A2202 | Start Date*: 2018-05-15 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multicenter, randomized, open-label, active-controlled, dose-range finding study to assess the pharmacodynamic parameters, safety and tolerability of MAA868 and its effect on thrombogenesis bioma... | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Suspended by CA) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002176-41 | Sponsor Protocol Number: 17HH4268 | Start Date*: 2019-09-03 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Imperial College of Science Technology and Medicine | ||||||||||||||||||||||||||||||||||||||
Full Title: PREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation (PRESTIGE-AF) | ||||||||||||||||||||||||||||||||||||||
Medical condition: Ischaemic stroke prevention in patients with atrial fibrillation and previous intracerebral haemorrhage | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) AT (Completed) FR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000794-23 | Sponsor Protocol Number: 49RC19_0034 | Start Date*: 2019-07-26 | |||||||||||||||||||||
Sponsor Name:CHU ANGERS | |||||||||||||||||||||||
Full Title: AntiCoagulants et COGnition (essai ACCOG) : Essai contrôlé randomisé en simple aveugle comparant les effets neurocognitifs du rivaroxaban par rapport à un antagoniste de la vitamine K | |||||||||||||||||||||||
Medical condition: fibrillation atriale non valvulaire | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000797-30 | Sponsor Protocol Number: SPI-IIT-002 | Start Date*: 2013-10-08 | |||||||||||||||||||||
Sponsor Name:Department of Medical Research, Odense University Hospital, Svendborg Hospital | |||||||||||||||||||||||
Full Title: Inhibition of aldosterone to diminish diffuse myocardial fibrosis in atrial fibrillation | |||||||||||||||||||||||
Medical condition: Paroxysmal and persistent atrial fibrillation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004847-37 | Sponsor Protocol Number: EDO-SP-01-2015 | Start Date*: 2017-10-05 | |||||||||||
Sponsor Name:FONDAZIONE G. D'ANNUNZIO, CHIETI | |||||||||||||
Full Title: A pilot study on Edoxaban for the resolution of left atrial thrombosis in patients with non-valvular atrial fibrillation | |||||||||||||
Medical condition: Non-Valvular Atrial Fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2021-000730-34 | Sponsor Protocol Number: ARMYDA-AMULET | Start Date*: 2021-06-28 | |||||||||||
Sponsor Name:FONDAZIONE TOSCANA GABRIELE MONASTERIO | |||||||||||||
Full Title: HeAd-to-head compaRison of single versus dual antiplatelet treatMent strategY after percutaneous left atrial appenDAge closure: A MULticenter, randomizEd sTudy the ARMYDA-AMULET study | |||||||||||||
Medical condition: Patients with atrial fibrillation undergoing percutaneous left atrial appendage closure with the Amulet device | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003444-24 | Sponsor Protocol Number: 1160.189 | Start Date*: 2014-11-21 | ||||||||||||||||||||||||||
Sponsor Name:Unilfarma - União Internacional de Lab. Farmacêuticos, Lda. | ||||||||||||||||||||||||||||
Full Title: Randomized, double-blind, Evaluation in secondary Stroke Prevention comparing the EfficaCy and safety of the oral Thrombin inhibitor dabigatran etexilate (110 mg or 150 mg, oral b.i.d.) versus acet... | ||||||||||||||||||||||||||||
Medical condition: A study to compare dabigatran etexilate to acetylsalicylic acid in preventing recurrent stroke for patients that already had a stroke caused by an embolus (clot). Despite testing, it is unknown wh... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) HU (Completed) IT (Completed) SE (Completed) SI (Completed) ES (Completed) CZ (Completed) SK (Completed) PL (Completed) HR (Completed) GR (Completed) EE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000504-18 | Sponsor Protocol Number: A01711 | Start Date*: 2011-05-10 | ||||||||||||||||||||||||||
Sponsor Name:Deutsches Herzzentrum München, Klinik für Herz- und Kreislauferkrankungen | ||||||||||||||||||||||||||||
Full Title: DABI-ADP-2: IMPACT OF DABIGATRAN AND PHENPROCOUMON ON CLOPIDOGREL MEDIATED ADP INDUCED PLATELET AGGREGATION IN PATIENTS WITH ATRIAL FIBRILLATION | ||||||||||||||||||||||||||||
Medical condition: Patients with atrial fibrillation and in indication for oral anticoagulation, who are currently receiving additionally clopidogrel for another medical condition, such as acute coronary syndrome and... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004121-16 | Sponsor Protocol Number: AC16141 | Start Date*: 2017-09-11 | |||||||||||
Sponsor Name:University of Edinburgh | |||||||||||||
Full Title: Start or STop Anticoagulants Randomised Trial (SoSTART) after spontaneous intracranial haemorrhage | |||||||||||||
Medical condition: Spontaneous Intracranial Haemorrhage (ICH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002353-38 | Sponsor Protocol Number: OHIRC-20150866 | Start Date*: 2017-08-31 | |||||||||||||||||||||
Sponsor Name:Ottawa Heart Institute Research Corporation (OHIRC) | |||||||||||||||||||||||
Full Title: The Optimal Anticoagulation for Enhanced Risk Patients Post-Catheter Ablation for Atrial Fibrillation Trial | |||||||||||||||||||||||
Medical condition: risk of stroke by atrial fibrillation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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