Pulmonary Regurgitation Clinical Trial
Official title:
Implantation of the SAPIEN™ Transcatheter Heart Valve (THV) in the Pulmonic Position
The purpose of this registry is to retrospectively and prospectively obtain clinical data in consecutively treated patients, in order to demonstrate that the commercially available Edwards SAPIEN Valve with the RF3 delivery system is a safe and effective treatment for patients with pulmonary regurgitation or stenosis.
Consecutive patient data should be collected at discharge, 6 months, 12 months and 2-5 years post-implant. ;
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