NCT04437303CompletedPhase 4
Periprocedural Continuation Versus Interruption of Oral Anticoagulant Drugs During Transcatheter Aortic Valve Implantation (POPular PAUSE TAVI)
Source: ClinicalTrials.gov · Last updated 31 May 2024
Brief summary (registry, in English)
Transcatheter aortic valve implantation (TAVI) is a rapidly growing treatment option for patients with aortic valve stenosis. Stroke is a feared complication of TAVI, with an incidence of around 4-5% in the first 30 days. Up to 50% of patients undergoing TAVI have an indication for oral anticoagulants (OAC) mostly for atrial fibrillation. OAC use during TAVI could increase bleeding complications, but interruption during TAVI may increase the risk for thromboembolic events (i.e. stroke, systemic embolism, myocardial infarction). Recent observational data suggest that periprocedural continuation of OAC is safe and might decrease the risk of stroke. Beside the potential reduction of thromboembolic events, continuation of OAC is associated with an evident clinical ancillary benefit for patients and staff. Since periprocedural OAC interruption not infrequently leads to misunderstanding and potentially dangerous situations, when patients are not properly informed before hospital admission or may experience difficulties with the interruption regimen. Hypothesis: Periprocedural continuation of oral anticoagulants is safe and might decrease thromboembolic complications without an increase in bleeding complications at 30 days
- Status (registry)
- Completed
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 858 (actual)
- First submitted
- 19 May 2020
- Start date
- 25 Nov 2020
- Primary completion date
- 21 Mar 2024
- Lead sponsor
- St. Antonius Hospital
- Diseases
- Coronary artery disease, Stroke
- NCT number
- NCT04437303
What you commit to
- Study type: Interventional · Phase 4
- Participants enrolled: 858
- From 25 Nov 2020 to the primary completion date, 21 Mar 2024
- 22 sites in 6 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients at high risk for thromboembolism for whom interruption of oral anticoagulants is no option, i.e.:
- Mechanical heart valve prosthesis
- \< 3 months after venous thromboembolism
- \< 6 months after transient ischemic attack or stroke in patients with atrial fibrillation
Other
- Intracardiac thrombus
Who the study is looking for
- Planned transfemoral or transsubclavian transcatheter aortic valve implantation procedure
- Uses oral anticoagulation at screening
- Provided written informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (22)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| O.L.V. Hospital Coordinator of this site? Confirm its status | Aalst | Belgium | Unknown status |
| A.S.Z. Hospital Coordinator of this site? Confirm its status | Aalst | Belgium | Unknown status |
| ZNA Middelheim Coordinator of this site? Confirm its status | Antwerp | Belgium | Unknown status |
| AZ Sint Jan Coordinator of this site? Confirm its status | Bruges | Belgium | Unknown status |
| East Limburg Hospital Coordinator of this site? Confirm its status | Genk | Belgium | Unknown status |
| University Hospital Leuven Coordinator of this site? Confirm its status | Leuven | Belgium | Unknown status |
| AZ Delta Coordinator of this site? Confirm its status | Roeselare | Belgium | Unknown status |
| Rigshospitalet, Copenhagen Coordinator of this site? Confirm its status | Copenhagen | Denmark | Unknown status |
| University Hospital Galway Coordinator of this site? Confirm its status | Galway | Ireland | Unknown status |
| Azienda Sanitaria Universitaria Integrata di Trieste Coordinator of this site? Confirm its status | Trieste | Italy | Unknown status |
| National Institute of Cardiac Surgery and Interventional Cardiology Coordinator of this site? Confirm its status | Luxembourg | Luxembourg | Unknown status |
| Amsterdam UMC Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Unknown status |
| Amphia Hospital Coordinator of this site? Confirm its status | Breda | Netherlands | Unknown status |
| UMC Groningen Coordinator of this site? Confirm its status | Groningen | Netherlands | Unknown status |
| Leiden University Medical Center Coordinator of this site? Confirm its status | Leiden | Netherlands | Unknown status |
| Maastricht UMC Coordinator of this site? Confirm its status | Maastricht | Netherlands | Unknown status |
| St. Antonius Ziekenhuis Coordinator of this site? Confirm its status | Nieuwegein | Netherlands | Unknown status |
| Radboud UMC Coordinator of this site? Confirm its status | Nijmegen | Netherlands | Unknown status |
| Erasmus MC Coordinator of this site? Confirm its status | Rotterdam | Netherlands | Unknown status |
| Haga Hospital Coordinator of this site? Confirm its status | The Hague | Netherlands | Unknown status |
| UMC Utrecht Coordinator of this site? Confirm its status | Utrecht | Netherlands | Unknown status |
| Isala Coordinator of this site? Confirm its status | Zwolle | Netherlands | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.