Ignite Creation Date:
2025-12-25 @ 12:32 AM
Ignite Modification Date:
2025-12-25 @ 10:40 PM
Study NCT ID:
NCT01424267
Status:
TERMINATED
Last Update Posted:
2012-10-11
First Post:
2011-08-23
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Zenith® LP Abdominal Aortic Aneurysm (AAA) Post-Market Registry
Sponsor:
Cook Group Incorporated
Organization:
Study Overview
Official Title:
Zenith® LP AAA Endovascular Graft Post-Market Registry
Status:
TERMINATED
Status Verified Date:
2012-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
The registry was discontinued due to significant resources required.
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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.
Detailed Description:
None
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: