Last updated: May 10, 2017
Sponsor: Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec
Overall Status: Completed
Phase
4
Condition
Stroke
Blood Clots
Congestive Heart Failure
Treatment
N/AClinical Study ID
NCT01559298
ARTE
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients undergoing a TAVI procedure with the Edwards SAPIEN XT valve (transfemoral ortransapical)
Exclusion
Exclusion Criteria:
Need for chronic anticoagulation treatment
Major bleeding within the 3 months prior to the TAVI procedure
Prior intracranial bleeding
Drug-eluting stent implantation within the year prior to the TAVI procedure
Allergy to clopidogrel and/or aspirin
Study Design
Total Participants: 178
Study Start date:
March 01, 2012
Estimated Completion Date:
March 31, 2016
Study Description
Connect with a study center
St-Paul's Hospital
Vancouver, British Columbia V6Z 1Y6
CanadaSite Not Available
IUCPQ
Quebec, G1V 4G5
CanadaSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.