Last updated on April 2017

Safety and Efficacy Study of Transcatheter Closure of Ostium Secundum ASDs


Brief description of study

Evaluate the safety and efficacy of the GORE® CARDIOFORM ASD Occluder in the percutaneous closure of ostium secundum atrial septal defects (ASDs)

Detailed Study Description

This is a prospective, multicenter, single-arm clinical study comparing outcomes with the GORE® CARDIOFORM ASD Occluder to performance goals derived from clinical investigation outcomes for devices indicated for ASD closure.

Clinical Study Identifier: NCT02985684

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Robert Sommer, MD

Columbia University Medical Center/New York Presbyterian Hospital
New York, NY United States
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