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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
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

Full criteria on ClinicalTrials.gov

Sites (22)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
O.L.V. Hospital
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AalstBelgiumUnknown status
A.S.Z. Hospital
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AalstBelgiumUnknown status
ZNA Middelheim
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AntwerpBelgiumUnknown status
AZ Sint Jan
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BrugesBelgiumUnknown status
East Limburg Hospital
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GenkBelgiumUnknown status
University Hospital Leuven
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LeuvenBelgiumUnknown status
AZ Delta
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RoeselareBelgiumUnknown status
Rigshospitalet, Copenhagen
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CopenhagenDenmarkUnknown status
University Hospital Galway
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GalwayIrelandUnknown status
Azienda Sanitaria Universitaria Integrata di Trieste
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TriesteItalyUnknown status
National Institute of Cardiac Surgery and Interventional Cardiology
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LuxembourgLuxembourgUnknown status
Amsterdam UMC
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AmsterdamNetherlandsUnknown status
Amphia Hospital
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BredaNetherlandsUnknown status
UMC Groningen
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GroningenNetherlandsUnknown status
Leiden University Medical Center
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LeidenNetherlandsUnknown status
Maastricht UMC
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MaastrichtNetherlandsUnknown status
St. Antonius Ziekenhuis
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NieuwegeinNetherlandsUnknown status
Radboud UMC
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NijmegenNetherlandsUnknown status
Erasmus MC
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RotterdamNetherlandsUnknown status
Haga Hospital
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The HagueNetherlandsUnknown status
UMC Utrecht
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UtrechtNetherlandsUnknown status
Isala
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ZwolleNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.