Transcatheter Aortic Valve Replacement Clinical Trial
Official title:
Antithrombotic Strategy Based on Clinical Events and 4D-CT for Patients After TAVR
This is a multicenter, open-label, randomized controlled study meant to test the superior efficacy of oral anticoagulation (OAC) therapy versus single antiplatelet therapy (SAPT) in patients after TAVR. Patients who accept successful TAVR will be randomized to receive either the OAC group (Vitamin-K antagonists) or the SAPT group (aspirin) for 6 months on a 1:1 ratio. After that, patients from both groups will be treated with single antiplatelet therapy (aspirin). All patients will be followed for 1 year to test the difference between net clinical benefits and bioprosthetic valve thrombosis diagnosed by 4D-CT.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05465655 -
Cara CDRM (Conduction Disturbance Risk Monitor) 2.0
|
N/A | |
Recruiting |
NCT04870424 -
Colchicine for Patients With Aortic Stenosis Undergoing Transcatheter Aortic Valve Replacement
|
Phase 3 | |
Completed |
NCT02758964 -
Evaluation of Cerebral Thrombembolism After TAVR
|
||
Recruiting |
NCT05758701 -
CT TAVR Abdomen Study
|
Phase 4 | |
Active, not recruiting |
NCT04281771 -
Assessment of Paravalvular Leak After TAVI by Hemodynamic Measurements and Cardiac MRI
|
N/A | |
Enrolling by invitation |
NCT06212050 -
Feasibility, Safety, and Effectiveness of the ACURATE neo2 Transcatheter Heart Valve for Severe Bicuspid Aortic Stenosis
|
||
Recruiting |
NCT04573049 -
The Effectiveness and Safety of Levosimendan in Patients With Severe Aortic Stenosis and Heart Failure Undergoing Transcatheter Aortic Valve Replacement
|
Phase 4 | |
Recruiting |
NCT05235555 -
EffecTAVI Registry
|
||
Completed |
NCT05082337 -
The SAVVY Guidewire in Transcatheter Aortic Valve Replacement Procedures
|
N/A | |
Completed |
NCT01627691 -
REPRISE II: REpositionable Percutaneous Replacement of Stenotic Aortic Valve Through Implantation of Lotus™ Valve System
|
N/A | |
Recruiting |
NCT05075590 -
Coronary Access After Supra-Annular THV Implantation
|
N/A | |
Completed |
NCT01651780 -
Open-label, Randomized Trial in Patients Undergoing TAVR to Determine Safety & Efficacy of Bivalirudin vs UFH
|
Phase 3 | |
Recruiting |
NCT05259241 -
ADAPT Transcatheter Aortic Valve Intervention (TAVI & Chronic Total Occlusion Percutaneous Coronary Intervention (CTO PCI)
|
N/A | |
Completed |
NCT04489914 -
Observational Study on the Application of High-Flow Therapy After Percutaneous Transfemoral Aortic Valve Replacement
|
||
Recruiting |
NCT03649594 -
Risk Stratification Post TAVI Using TEG
|
||
Completed |
NCT04659538 -
The CAPTIS® Study - Embolic Protection in TAVR
|
N/A | |
Recruiting |
NCT04107038 -
Monitored Anesthesia Care vs. General Anesthesia for Transcatheter Aortic Valve Replacement
|
N/A | |
Withdrawn |
NCT04268160 -
GPx Activity in Subjects With Aortic Stenosis Undergoing TAVR
|
||
Recruiting |
NCT02812953 -
Biological Collection and Registry of Patients Who Will Have a TAVR (Transcatheter Aortic Valve Replacement) Intervention
|
||
Recruiting |
NCT05217888 -
The Sentinel Registry
|