Atrial Fibrillation Clinical Trial
Official title:
China REgistry of WATCHMAN Left Atrial Appendage Closure for Non-valvular Atrial Fibrillation
This registry is designed to observe the safety and effectiveness of WATCHMAN left atrial appendage closure technology in a Chinese population.
In this prospective, multi-center, single arm observational study, 413 patients with non-valvular atrial fibrillation intended to be implanted with a WATCHMAN device based on real clinical practice will be enrolled. Enrolled subjects will be followed up for 5 years.Primary endpoints include stroke, systematic embolism, cardiovascular death, and procedure or device related complications, etc. ;
Observational Model: Cohort, Time Perspective: Prospective
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