Brief Title
Zenith® Spiral-Z® AAA Iliac Leg Graft Post-market Registry
Official Title
Zenith® Spiral-Z® AAA Iliac Leg Graft Post-market Registry
Brief Summary
The purpose of this registry is to obtain case reports of physician experience with the Spiral-Z® graft under routine clinical care.
Study Type
Observational
Primary Outcome
Assess short term and longer term outcomes, including outcomes related to patency, of the Zenith® Spiral-Z® AAA Iliac Leg Graft.
Condition
Abdominal Aortic Aneurysm
Intervention
Iliac Leg Graft
Study Arms / Comparison Groups
Abdominal aortic aneurysm
Description:
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Recruitment Status
Device
Estimated Enrollment
600
Start Date
March 2012
Completion Date
March 2016
Primary Completion Date
March 2016
Eligibility Criteria
Inclusion Criteria: - Patient is implanted with Zenith® Spiral-Z® AAA Iliac Leg Graft. Exclusion Criteria: - Patients for whom this device would not normally be considered standard of care.
Gender
All
Ages
N/A - N/A
Accepts Healthy Volunteers
No
Contacts
Thomas Lindsay, ,
Location Countries
Canada
Location Countries
Canada
Administrative Informations
NCT ID
NCT01540643
Organization ID
11-015
Responsible Party
Sponsor
Study Sponsor
Cook Group Incorporated
Study Sponsor
Thomas Lindsay, Principal Investigator, Toronto General Hospital
Verification Date
January 2017