Brief Title
Zenith® LP Abdominal Aortic Aneurysm (AAA) Post-Market Registry
Official Title
Zenith® LP AAA Endovascular Graft Post-Market Registry
Brief Summary
A registry to collect additional prospective intra-operative and follow-up information on physician use of the CE-marked Zenith® Low Profile Abdominal Aortic Aneurysm (AAA) Endovascular Graft under routine clinical care.
Study Type
Observational
Primary Outcome
graft patency and aneurysm exclusion
Condition
Abdominal Aortic Aneurysm
Intervention
Zenith® Low Profile AAA Endovascular Graft
Study Arms / Comparison Groups
1
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
76
Start Date
July 2010
Completion Date
August 2012
Primary Completion Date
August 2012
Eligibility Criteria
Inclusion Criteria: - Patient is implanted with Zenith® Low Profile AAA Endovascular 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
, ,
Location Countries
Austria
Location Countries
Austria
Administrative Informations
NCT ID
NCT01424267
Organization ID
10-006
Responsible Party
Sponsor
Study Sponsor
Cook Group Incorporated
Study Sponsor
, ,
Verification Date
October 2012