Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI).

This study is currently recruiting participants. (see Contacts and Locations)
Verified October 2015 by Medtronic Cardiovascular
Information provided by (Responsible Party):
Medtronic Cardiovascular Identifier:
First received: April 24, 2012
Last updated: October 20, 2015
Last verified: October 2015
No Study Results Posted on for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: No date given
  Estimated Primary Completion Date: August 2016 (Final data collection date for primary outcome measure)
No publications provided by Medtronic Cardiovascular

Publications automatically indexed to this study by Identifier (NCT Number):