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Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement

Severe Aortic Stenosis Clinical Trial

Official title:
Medtronic CoreValve® U.S. Pivotal Trial

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01240902
Study type Interventional
Source Medtronic Cardiovascular
Contact
Status Completed
Phase N/A
Start date December 10, 2010
Completion date May 15, 2019
View Details
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