drugset / Trial / NCT04684212

Can the Lambre Device Occlude IRRegular And Large Appendages in Patients With Non-Valvular AF

NCT04684212 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective is to demonstrate the safety and efficacy of the implantation of the LAmbre PlusTM device in patients with large or irregularly shaped appendages with non-valvular atrial fibrillation who are at increased risk for stroke and systemic embolism compared to oral anticoagulation (OAC).

Timeline

Start
2024-06-01
Primary completion
2024-06-01
Completion
2024-07-11

Outcome

Outcome not reported

Stopped (Business): “Lack of Funding”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Apixiban Unknown — Oral
Comparator Betrixaban Small molecule — Oral
Comparator Dabigatran Unknown — Oral
Comparator Edoxaban Small molecule — Oral
Comparator Rivaroxaban Other / unclassified — Oral
Comparator Warfarin Small molecule — Oral