CoreValve® System Australia/New Zealand Clinical Study

NACompletedINTERVENTIONAL
Enrollment

634

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

October 31, 2014

Study Completion Date

September 30, 2016

Conditions
Aortic Valve Stenosis
Interventions
DEVICE

Medtronic CoreValve® System

The Medtronic CoreValve® System device is designed to replace the native aortic valve without the requirement for open heart surgery and without concomitant surgical removal of the failed native valve in patients with symptomatic severe aortic stenosis who have an elevated surgical risk

Trial Locations (10)

3004

Epworth Hospital, Melbourne

Unknown

St. Vincents Sydney, Darlinghurst

Prince Charles Hospital, Chermside

Royal Adelaide Hospital, Adelaide

Monash Hospital, Clayton

St. Vincent's Melbourne, Fitzroy

Alfred Hospital, Melbourne

Royal Perth Hospital, Perth

Mercy Hospital, Auckland

Waikato Hospital, Hamilton

Sponsors
All Listed Sponsors
collaborator

Medtronic Australasia

UNKNOWN

lead

Medtronic Cardiovascular

INDUSTRY

NCT01015612 - CoreValve® System Australia/New Zealand Clinical Study | Biotech Hunter | Biotech Hunter