Cook Iliac Branch Graft Post-market Registry

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01055275

Enrollment

Registered

2010-01-25

Start date

2010-09-30

Completion date

2012-08-31

Last updated

2013-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Aneurysm, Iliac Aneurysm

Keywords

iliac aneurysm, aortic aneurysm, endovascular grafts

Brief summary

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.

Interventions

DEVICEImplantation with a Cook Iliac Branch Graft

Treatment of an aortic, aorto-iliac or iliac aneurysm with a CE-marked Cook Iliac Branch Graft.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame
Internal iliac artery patency	1 year
Aneurysm Exclusion	1 year

Secondary

Measure	Time frame
Rupture	1 year
Death	1 year
Major Complications	1 year
Success Measures	1 year
Conversion	1 year

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026