OPTION
This Study is
No Longer Enrolling
Description
This study is a prospective, randomized, multi-center, global investigation to determine if left atrial appendage closure with the WATCHMAN FLX Device is a reasonable alternative to oral anticoagulation in patients after AF ablation.
Details
Age
Adult
Type of Study
Treatment
Scope
National
Locations
Medical Center of the Rockies
Study ID
Protocol Number: 20-6502
More information available at ClinicalTrials.gov: NCT03795298
Categories
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