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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
Phase
Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.
Type of Study
Treatment
Scope
National
Location
Medical Center of the Rockies
Principal Investigator
Russell Heath
Study ID
Protocol Number: 20-6502
ClinicalTrials.gov: NCT03795298
Categories
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