- Trials with a EudraCT protocol (122)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
122 result(s) found for: Rivaroxaban.
Displaying page 4 of 7.
EudraCT Number: 2016-002291-27 | Sponsor Protocol Number: RIVAR-CTP-01 | Start Date*: 2016-11-07 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Randomized trial of aspirin versus rivaroxaban after replacement of the aortic valve with a biological valve prosthesis | |||||||||||||
Medical condition: Aortic valve stenosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001534-19 | Sponsor Protocol Number: APHP200015 | Start Date*: 2021-05-21 |
Sponsor Name:AP-HP/DRCI | ||
Full Title: Direct oral Anticoagulants for Prevention of lEft ventRIcular Thrombus after anterior acute myocardial InFarction | ||
Medical condition: Left ventricular (LV) thrombus after acute myocardial infarction (AMI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001723-12 | Sponsor Protocol Number: ARIVA_venous | Start Date*: 2020-05-28 |
Sponsor Name:Universitätsspital Zürich, Klinik für Angiologie | ||
Full Title: Aspirin® plus rivaroxaban versus rivaroxaban alone for the prevention of venous stent thrombosis in patients with post-thrombotic syndrome | ||
Medical condition: Post-thrombotic syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003299-11 | Sponsor Protocol Number: RD2018-41 | Start Date*: 2018-10-22 | |||||||||||
Sponsor Name:East and North Hertfordshire NHS Trust | |||||||||||||
Full Title: Can Very Low Dose Rivaroxaban (VLDR) in addition to dual antiplatelet therapy (DAPT) improve thrombotic status in acute coronary syndrome (ACS) | |||||||||||||
Medical condition: Acute Coronary Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001062-15 | Sponsor Protocol Number: BAY59-7939/16320 | Start Date*: 2013-06-13 | ||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
Full Title: An open-label, international, multicenter, interventional study exploring the efficacy of once-daily oral rivaroxaban (BAY 59-7939) for the treatment of left atrial/left atrial appendage thrombus i... | ||||||||||||||||||
Medical condition: Atrial Fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) BG (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000610-10 | Sponsor Protocol Number: RivAsA | Start Date*: 2020-01-27 | ||||||||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
Full Title: Effects of low-dose Rivaroxaban combined with low-dose Aspirin versus low-dose aspirin alone on in vivo platelet Activation, endothelial function and inflammation in type 2 diabetic patients with s... | ||||||||||||||||||
Medical condition: type 2 diabetic patients with stable peripheral or carotid artery disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: 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: 2015-001478-16 | Sponsor Protocol Number: CONKO-011_AIO-SUP-0115/ass. | Start Date*: 2016-01-05 |
Sponsor Name:AIO-Studien-gGmbH | ||
Full Title: Rivaroxaban in the treatment of venous thrombembolism (VTE) in cancer patients – a randomized phase III Study | ||
Medical condition: Tumor patients with active cancer and newly diagnosed thrombembolic events were randomised to receive either Rivaroxaban or the standard treatment with low-molecular heparine | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: View results |
EudraCT Number: 2013-004575-13 | Sponsor Protocol Number: TRAPS-1.5 | Start Date*: 2014-10-29 |
Sponsor Name:Dipartimento di Scienze Cardiologiche, Toraciche e Vascolari-Università di Padova | ||
Full Title: A prospective, randomized clinical trial comparing Rivaroxaban vs warfarin in high risk patients with antiphospholipid syndrome (TRAPS). | ||
Medical condition: THROMBOEMBOLISM PREVENTION | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005589-37 | Sponsor Protocol Number: RMRHS0095 | Start Date*: 2013-03-08 | ||||||||||||||||
Sponsor Name:University of Warwick | ||||||||||||||||||
Full Title: select-d: Anticoagulation Therapy in SELECTeD Cancer Patients at Risk of Recurrence of Venous Thromboembolism | ||||||||||||||||||
Medical condition: Venous Thromboembolism and Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000353-26 | Sponsor Protocol Number: SAFE-SSPE | Start Date*: 2021-09-20 |
Sponsor Name:Bern University Hospital | ||
Full Title: Clinical Surveillance vs. Anticoagulation for Low-risk Patients with Isolated Subsegmental Pulmonary Embolism: A Multicenter Randomized Placebo-Controlled Non-Inferiority Trial | ||
Medical condition: Isolated subsegmental pulmonary embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001443-31 | Sponsor Protocol Number: 1801 | Start Date*: 2018-11-21 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: DOAC Levels prior to Incision study: DALI study | ||
Medical condition: No medical condition will be investigated. This study will only investigate DOAC levels during surgery. Patients who use DOACs are patients with venous thrombosis and atrial fibrillation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019764-36 | Sponsor Protocol Number: SAP-02 | Start Date*: 2011-02-03 | |||||||||||
Sponsor Name:JOSEP ORDI-ROS | |||||||||||||
Full Title: RIVAROXABAN VERSUS ACENOCUMAROL EN LA PROFILAXIS SECUNDARIA DEL SÍNDROME ANTIFOSFOLÍPIDO:UN ESTUDIO MULTICÉNTRICO, PROSPECTIVO Y RANDOMIZADO. | |||||||||||||
Medical condition: Sindrome Antifosfolípido | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004784-53 | Sponsor Protocol Number: APHP200002 | Start Date*: 2022-07-19 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux de Paris | |||||||||||||
Full Title: Rivaroxaban versus standard of care for patients with excessive atrial ectopy or short atrial runs and high embolism risk SHORT RUN AF | |||||||||||||
Medical condition: excessive atrial ectopy or short atrial runs and high embolism risk | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003621-28 | Sponsor Protocol Number: 5072018 | Start Date*: 2019-07-23 | |||||||||||||||||||||
Sponsor Name:IUCPQ | |||||||||||||||||||||||
Full Title: Short-Term Anticoagulation versus Antiplatelet Therapy for Preventing Device Thrombosis Following Left Atrial Appendage Closure. The ANDES study. | |||||||||||||||||||||||
Medical condition: Device thrombosis at 2 months and 12 months after left atrial appendage closure (LAAC) Ischemic events (stroke, TIA) at 2-month and 1-, 2-, 3-, 4-and 5-year follow-up Bleeding events at 2-month an... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002529-39 | Sponsor Protocol Number: PHRC2015-07 | Start Date*: 2017-08-30 |
Sponsor Name:CHU Angers | ||
Full Title: Intérêt de l’administration de charbon Activé pour les patients ayant un geste invasif reporté dû à un traitement Anticoagulant Oral Direct | ||
Medical condition: fibrillation auriculaire ou une maladie veineuse thromboembolique | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002084-20 | Sponsor Protocol Number: Version_1.0_MP_and_anticoagulants | Start Date*: 2011-07-28 |
Sponsor Name:Medizinische Universität Wien; Universitätsklinik für Klinische Pharmakologie | ||
Full Title: A prospective, randomized, controlled open-label trial to investigate the effects of 10mg rivaroxaban or 110mg dabigatran on microparticle formation in critically ill patients compared to age-& sex... | ||
Medical condition: The effect of the used IMPs should be investigated in critically ill patients and healthy subjects | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004913-11 | Sponsor Protocol Number: 111075 | Start Date*: 2021-02-18 |
Sponsor Name:Radboudumc | ||
Full Title: genotype-guided strategy for antithrombotic treatment versus conventional clopidogrel therapy in peripheral arterial disease’ | ||
Medical condition: Symptomatic or stable pheripheral artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001190-40 | Sponsor Protocol Number: P110150 | Start Date*: 2018-05-16 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005110-17 | Sponsor Protocol Number: PhRisCo-study | Start Date*: 2021-10-07 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA MAGGIORE DELLA CARITà DI NOVARA | ||||||||||||||||||
Full Title: Pharmacodynamic and pleiotropic effects of Rivaroxaban in Coronary Artery Disease and Atrial Fibrillation | ||||||||||||||||||
Medical condition: stable CAD; history of atrial fibrillation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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