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Terminated Phase 2 Interventional

Safety Study for the Treatment of Abdominal Aortic Aneurysms

ClinicalTrials.gov ID: NCT00610090

Public ClinicalTrials.gov record NCT00610090. 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 24, 2026, 10:43 PM EDT

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

Official title

A Phase II, Single-arm, Prospective Study of the Safety of the UniFit Aorto-uni-iliac Endoluminal Stent Graft for the Repair of Abdominal Aortic Aneurysms

Brief summary

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

The primary study objective, at this time, is to follow out to 5 years post implant the safety of already enrolled subjects who were treated with the UniFit Aorto-uni-iliac (AUI) Endoluminal Stent Graft (the "study device") for the repair of abdominal aortic aneurysms (AAAs).

Study identification

NCT ID
NCT00610090
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Duke Vascular, Inc.
Industry
Enrollment
71 participants

Conditions and interventions

Interventions

Device

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
May 2007 (Type not available)
Primary completion
Dec 2015 (Estimated)
Completion
Dec 2015 (Estimated)
Last update posted
Aug 25, 2015

2007 – 2015

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Loma Linda VA Loma Linda California 92354 —
UCLA Medical Center Torrance California 90502 —
Christiana Hospital Newark Delaware 19713 —
Florida Hospital Orlando Florida 32803 —
Sacred Heart Hospital Pensacola Florida 32504 —
Emory University Atlanta Georgia 30322 —
Savannah Vascular Institute Savannah Georgia 31404 —
Indiana University Hospital Indianapolis Indiana 46206 —
Iowa Heart Center Des Moines Iowa 50266 —
University of Massachusetts Medical School Worcester Massachusetts 01655 —
William Beaumont Hospital Royal Oak Michigan 48073 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Englewood Hospital Englewood New Jersey 07631 —
Albany Medical Center Hospital Albany New York 12208 —
Dotter Interventional Institute Portland Oregon 97239 —
Scott and White Hospital Temple Texas 76508 —
Inova Fairfax Hospital Fairfax Virginia 22042 —
Sentara Healthcare, Vascular and Transplant Specialists Norfolk Virginia 23507 —
Southwest Washington Medical Center Vancouver Washington 98664 —

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 NCT00610090, 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 Aug 25, 2015 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00610090 live on ClinicalTrials.gov.

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