About this trial
The POPular ATLANTIS trial aims to investigate CT-guided antithrombotic therapy compared to lifelong single antiplatelet therapy after a transcatheter aortic valve implantation (TAVI) procedure. Only patients without an indication for anticoagulants will be included in this trial. Currently, lifelong single antiplatelet therapy (mostly aspirin) is considered the standard of care for these patients. However, this approach poses a bleeding risk with only a minimal reduction in thromboembolic events.
After 3 months, a CT scan will be conducted to assess the presence of thrombosis on the newly implanted TAVI valve. Based on the results of a 4D CT scan, the decision will be made whether the patient should receive no anticoagulant or antithrombotic therapy with apixaban. CT-guided antithrombotic therapy holds the potential for a greater reduction in thromboembolic events without increasing the bleeding risk.
Eligibility criteria
Qualifiers
Successful TAVI (according to the VARC-3 criteria)10 with any approved device
Ability to understand and to comply with the study protocol
Written informed consent
Disqualifiers
Existing indication for oral anticoagulation (e.g. atrial fibrillation, obstructive valve thrombosis detected by echocardiography prior to inclusion)
Existing indication for dual antiplatelet therapy at three months after TAVI (rare at this time point)
Creatinine clearance <15 mL/min (based on the CKD-EPI formula) or on renal replacement therapy
Trial design
Treatments tested in this trial
- CT guided strategy
Treatment groups
Sponsors and collaborators
St. Antonius Hospital
Lead sponsor
ZonMw: The Netherlands Organisation for Health Research and Development
Collaborator
Pitié-Salpêtrière Hospital
Collaborator