Cook Iliac Branch Graft Post-market Registry

NCT ID: NCT01055275

Last Updated: 2013-06-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

2 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-09-30

Study Completion Date

2012-08-31

Brief Summary

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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.

Detailed Description

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Conditions

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Iliac Aneurysm Aortic Aneurysm

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cook Iliac Branch Graft

Patients implanted with a Cook Iliac Branch Graft

Implantation with a Cook Iliac Branch Graft

Intervention Type DEVICE

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

Interventions

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Implantation with a Cook Iliac Branch Graft

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

Intervention Type DEVICE

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cook Group Incorporated

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Vincent Riambau, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospital Clinic, Barcelona, Spain

Locations

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Hospital Clinic

Barcelona, , Spain

Site Status

Countries

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Spain

Other Identifiers

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09-016

Identifier Type: -

Identifier Source: org_study_id

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