Aortic Aneurysm Clinical Trial
Official title:
Cook Iliac Branch Graft Post-market Registry
Verified date | June 2013 |
Source | Cook |
Contact | n/a |
Is FDA regulated | No |
Health authority | Spain: Spanish Agency of Medicines |
Study type | Observational |
The Cook Iliac Branch Graft Post-market Registry will obtain case reports of physician experience with a CE-marked Cook Iliac Branch Graft to further confirm device safety and performance.
Status | Terminated |
Enrollment | 2 |
Est. completion date | August 2012 |
Est. primary completion date | August 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - CE-Marked Cook Iliac Branch Graft (e.g., Zenith® Branch Endovascular Graft-Iliac Bifurcation, Zenith® Helical Branch Endovascular Graft) - Registry data are de-identified with respect to patient. Exclusion Criteria: - Patient for whom this device would not normally be considered standard of care. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Spain | Hospital Clinic | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Cook |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Internal iliac artery patency | 1 year | No | |
Primary | Aneurysm Exclusion | 1 year | No | |
Secondary | Death | 1 year | No | |
Secondary | Conversion | 1 year | No | |
Secondary | Rupture | 1 year | No | |
Secondary | Success Measures | 1 year | No | |
Secondary | Major Complications | 1 year | No |
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