WATCHMAN FLX Real World Evidence Protocol

Primary Objective

To collect real world clinical outcomes data for patients who are implanted with the WATCHMAN FLX device in a commercial clinical setting.

This Study is
No Longer Enrolling

Description

NA

Details
Age

Adult

Eligibility

NA

NA

Type of Study

Observational

Scope

National

Locations

Memorial Hospital Central

Study ID

Protocol Number: 22-0299

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