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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