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Clinical Trial Summary

This registry is designed to observe the safety and effectiveness of WATCHMAN left atrial appendage closure technology in a Chinese population.


Clinical Trial Description

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. ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT03014557
Study type Observational [Patient Registry]
Source Fu Wai Hospital, Beijing, China
Contact Zhengqin Zhai, MD PhD
Email 384358085@qq.com
Status Recruiting
Phase N/A
Start date November 2016
Completion date December 2023

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