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First received: September 29, 2022

Clinical Trial: Watchman FLX Pro CT Pilot Study

Study Status: COMPLETED

Recruit Status: COMPLETED

Condition: Non-valvular Atrial Fibrillation (AF)

Study Type: INTERVENTIONAL


Official Title: A Pilot Study to Assess WATCHMAN FLX™ Pro Implants by Cardiac Computed Tomography, Magnetic Resonance Imaging and Transesophageal Echocardiography: WATCHMAN FLX Pro CT

Brief Summary: The primary objective of this study is to measure device tissue coverage post-implantation of the WATCHMAN FLX™ Pro Left Atrial Appendage Closure (LAAC) Device (WATCHMAN FLX Pro) using the serial advanced imaging modalities of cardiac computed tomography (CT) and transesophageal echocardiography (TEE) and assess its relationship, if any, to clinical events.

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