- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Aortic Valve Stenosis.
Displaying page 2 of 3.
| EudraCT Number: 2005-002580-85 | Sponsor Protocol Number: 3d | Start Date*: 2005-08-08 |
| Sponsor Name:Rigshospitalet | ||
| Full Title: Acute haemodynanic effects of Treatment with ACE inhibitores in patients with severe Aortic Stenosis | ||
| Medical condition: Aortic valve stenosis is a reduction of the aortic valve orifice to a degree where emptying of the left ventricule is compromised. The two major causes for aortic valve stenosis is calcific valve d... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005306-39 | Sponsor Protocol Number: VitaminKStudy | Start Date*: 2009-06-29 | |||||||||||
| Sponsor Name:RWTH Aachen University, represented by the rector, himself represented by Clinical Trial Center Aachen (CTC-A) | |||||||||||||
| Full Title: Food supplementation with Vitamin K for MGP-activation and inhibition of progression of aortic valve calcification | |||||||||||||
| Medical condition: progression of aortic valve calcification | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001777-33 | Sponsor Protocol Number: EARTH-TAVR01 | Start Date*: 2016-09-01 | |||||||||||
| Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
| Full Title: EVALUATION OF CEREBRAL THROMBOEMBOLISM AFTER TAVR | |||||||||||||
| Medical condition: Patients with severe aortic stenosis that require Transcatheter aortic valve replacement are at risk for stroke. This study is to evaluate the occurrence and extent of cerebral embolization (total... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001975-30 | Sponsor Protocol Number: BAY59-7939/17938 | Start Date*: 2016-01-12 | |||||||||||
| Sponsor Name:Bayer AG | |||||||||||||
| Full Title: Global multicenter, open-label, randomized, event-driven, active-controlled study comparing a rivAroxaban-based antithrombotic strategy to an antipLatelet-based strategy after transcatheter aortIc ... | |||||||||||||
| Medical condition: Patients with severe aortic stenosis that require Transcatheter aortic valve replacement are at risk of thrombus formation. Rivaroxaban (oral-anticoagulant) may reduce this risk, without increasing... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) BE (Prematurely Ended) NO (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) SE (Prematurely Ended) NL (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) CZ (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004271-14 | Sponsor Protocol Number: DAPAS | Start Date*: 2021-12-06 | |||||||||||
| Sponsor Name:Aarhus University Hospital, department of Cardiology | |||||||||||||
| Full Title: Effect of Dapagliflozin on myocardial and renal function following aortic valve stenosis intervention | |||||||||||||
| Medical condition: Patients with aortic stenosis undergoing trans catheter aortic valve replacement. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000704-25 | Sponsor Protocol Number: PASP01 | Start Date*: 2017-02-28 |
| Sponsor Name:Queen Mary University of London | ||
| Full Title: Prevention of Aortic Stenosis Pilot Trial | ||
| Medical condition: Aortic Stenosis. It is caused by the build-up of calcium phosphate crystals on the aortic valve (aortic sclerosis). Progressive valve narrowing (stenosis) leads to symptoms (chest pain, syncope or ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-002037-11 | Sponsor Protocol Number: IIISAS | Start Date*: 2019-10-10 | |||||||||||
| Sponsor Name:Oslo University Hospital | |||||||||||||
| Full Title: Intravenous Iron supplement for Iron deficiency in patients with Severe Aortic Stenosis | |||||||||||||
| Medical condition: Iron deficiency, aortic stenosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001425-26 | Sponsor Protocol Number: REDOX19032019 | Start Date*: 2019-07-04 |
| Sponsor Name:Thoraxcentrum Erasmus MC | ||
| Full Title: Rotterdam Edoxaban Leaflet Evaluation in Patients after Transcatheter Aortic Valve Implantation | ||
| Medical condition: aortic stenosis | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-005224-32 | Sponsor Protocol Number: OCMR 06.01 | Start Date*: 2008-12-16 |
| Sponsor Name:University of Oxford | ||
| Full Title: A randomised controlled trial of the angiotensin converting enzyme inhibitor ramipril in asymptomatic aortic stenosis | ||
| Medical condition: Aortic stenosis of at least moderate degree (peak velocity >=3.0m/sec or aortic valve area <1.5cm2) | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005784-24 | Sponsor Protocol Number: MEIXO-VALV-001 | Start Date*: 2012-06-14 |
| Sponsor Name:Andres Iñiguez Romo | ||
| Full Title: Dual antiplatelet therapy versus oral anticoagulation for a short time to prevent cerebral embolism after percutaneous aortic valve implantation. Multicenter randomized clinical trial. | ||
| Medical condition: Evaluate the efficacy of dual antiplatelet therapy versus oral anticoagulation for primary prevention of cerebral thromboembolism at three months after percutaneous aortic valve implantation (TAVI). | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001147-31 | Sponsor Protocol Number: 140481 | Start Date*: 2013-06-06 |
| Sponsor Name:Aarhus University Hospital, Department of Cardiology | ||
| Full Title: Aortic Valve Stenosis and Myocardial Efficiency – a Prognostic Marker and a Target for Intervention? | ||
| Medical condition: Aortic stenosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001930-34 | Sponsor Protocol Number: 170674-3479 | Start Date*: 2005-11-25 |
| Sponsor Name:Department of Cardiology, Odense University Hospital | ||
| Full Title: Left ventricular reverse remodelling after aortic valve replacement in severe valvular aortic stenosis - effect of blockade of the angiotensin-II receptor | ||
| Medical condition: Patients with severe aortic valve stenosis treated with Aortic Valve Replacement (AVR) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001554-61 | Sponsor Protocol Number: ACASA-TAVI-2.1 | Start Date*: 2021-08-19 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Anti-Coagulation versus AcetylSalicylic Acid after Transcatheter Aortic Valve Implantation (ACASA-TAVI) | ||
| Medical condition: Patients with aortic stenosis undergoing transcatheter aortic valve implantation. | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004860-23 | Sponsor Protocol Number: REACTIC2019-HAC | Start Date*: 2020-05-22 |
| Sponsor Name:Andres Iñiguez Romo | ||
| Full Title: REACTIC-TAVI TRIAL: Platelet REACtivity according to TICagrelor dose after Trancathter Aortic Valve Implantation. A pilot study. | ||
| Medical condition: Patients with severe aortic stenosis submitted for Transcatheter Aortic Valve Implantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004559-36 | Sponsor Protocol Number: 1 | Start Date*: 2006-03-23 |
| Sponsor Name:Abteilung für Herz-Thorax-Gefäß Anästhesie & Intensivmedizin (HTG) | ||
| Full Title: Desmopressin in Acquired von Willebrand Syndrome caused by Aortic Valve Stenosis | ||
| Medical condition: Acquired type 2A von Willebrand syndrome is common in patients with severe aortic valve stenosis (AS). It originates from the mechanical obstruction of blood flow and the consecutive proteolysis of... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003861-39 | Sponsor Protocol Number: GLUCOTAVI | Start Date*: 2023-03-07 |
| Sponsor Name:JUAN MIGUEL RUIZ NODAR | ||
| Full Title: Glucocorticoid treatment in patients undergoing TAVI to reduce the incidence of atrioventricular block and pacemaker implantation | ||
| Medical condition: aortic stenosis | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001808-57 | Sponsor Protocol Number: BICATOR | Start Date*: 2015-11-27 | |||||||||||
| Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | |||||||||||||
| Full Title: Assessment of atorvastatin efficacy on the progression of aortic dilatation and valvular degeneration in patients with bicuspid aortic valve (BICATOR) | |||||||||||||
| Medical condition: Valve Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002376-95 | Sponsor Protocol Number: RRK3535 | Start Date*: 2009-01-05 |
| Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||
| Full Title: Myocardial protection with Perhexiline in Left Ventricular Hypertrophy | ||
| Medical condition: Patients with left ventricular hypertrophy undergoing aortic valve surgery (with or without coronary artery surgery) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004144-20 | Sponsor Protocol Number: CHUBX2014/24 | Start Date*: 2015-11-17 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: Safety profile evaluation of TICagrelor Alone compared to a combination of lysine acetylsalicylate - Clopidogrel in the context of Transcatheter Aortic Valve Implantation (TAVI) | ||
| Medical condition: Aortic valve stenosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001817-20 | Sponsor Protocol Number: NL73805.100.20 | Start Date*: 2021-05-07 |
| Sponsor Name:St. Antonius Hospital Nieuwegein, The Netherlands | ||
| Full Title: Periprocedural continuation versus interruption of oral anticoagulant drugs during transcatheter aortic valve implantation | ||
| Medical condition: Thromboembolic, bleeding and vascular complications after transcatheter aortic valve implantation in patients using oral anticoagulants | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) DK (Completed) IT (Completed) | ||
| Trial results: View results | ||
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