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Completed Not applicable Interventional Results available

PRESERVE-Zenith® Iliac Branch System Clinical Study

ClinicalTrials.gov ID: NCT01208415

Public ClinicalTrials.gov record NCT01208415. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 2:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The PRESERVE-Zenith® Iliac Branch System Clinical Study is a clinical trial to study the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the Zenith® Connection Endovascular Stent/ConnectSX™ covered stent in the treatment of aorto-iliac and iliac aneurysms.

Study identification

NCT ID
NCT01208415
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Cook Group Incorporated
Industry
Enrollment
40 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2011 (Type not available)
Primary completion
Oct 2012 (Actual)
Completion
Oct 10, 2017 (Actual)
Last update posted
Apr 4, 2018

2011 – 2017

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
VA Palo Alto HCS Palo Alto California 94304 —
Stanford University Medical Center Stanford California 94305 —
Christine E. Lynn Heart and Vascular Institute Boca Raton Florida 33431 —
University of Florida Gainesville Florida 32610 —
Emory University Atlanta Georgia 30322 —
University of Massachusetts Worcester Massachusetts 01655 —
William Beaumont Hospital Royal Oak Michigan 48073 —
Mayo Clinic Rochester Minnesota 55905 —
Washington University School of Medicine St Louis Missouri 63110 —
Mercy Hospital East Communities St Louis Missouri 63141 —
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756 —
Columbia University Medical Center New York New York 10032 —
Weill Cornell Medical Center New York New York 10065 —
University of North Carolina Chapel Hill North Carolina 27599 —
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Allegheny General Hospital Pittsburgh Pennsylvania 15212 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
University of Virginia Charlottesville Virginia 22908 —
Aurora St. Luke's Hospital Milwaukee Wisconsin 53215 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01208415, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2018 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01208415 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →