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Study category: Heart and Blood Conditions

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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

Russell Heath

Study ID

Protocol Number: 20-6502

ClinicalTrials.gov: NCT03795298

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