Corevalve Extreme Risks Patients

Investigator: Neal Kleiman, MD

Study Coordinator: LaShawna Green

Status: Open Not Enrolling Number: NCT01240902

Phone: 713.441.6548

Protocol Number: Pro00005138


The purpose of the study is to evaluate the safety and efficacy of the Medtronic CoreValve® System in the treatment of symptomatic severe aortic stenosis in subjects who have a predicted high risk for aortic valve surgery and/or very high risk for aortic valve surgery.
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