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Completed Not applicable Interventional Results available

Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System

ClinicalTrials.gov ID: NCT00705718

Public ClinicalTrials.gov record NCT00705718. 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 Jul 21, 2026, 7:09 AM EDT

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

Official title

Endurant Stent Graft System US Clinical Study

Study identification

NCT ID
NCT00705718
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Cardiovascular
Industry
Enrollment
194 participants

Conditions and interventions

Interventions

  • Endurant Stent Graft System Device

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 31, 2008
Primary completion
Aug 31, 2012
Completion
Sep 25, 2016
Last update posted
Nov 2, 2021

2008 – 2016

United States locations

U.S. sites
30
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
University of Alabama Hospitals Birmingham Alabama 35294
Arizona Heart Institute Phoenix Arizona 85006
Stanford University Medical Center Stanford California 94305
Sarasota Memorial Hospital Sarasota Florida 34239
Emory University Hospital Atlanta Georgia 30322
Wellstar Kennestone Hospital Marietta Georgia 30106
Northwestern Memorial Hospital Chicago Illinois 60611
Good Samaritan Hospital Downers Grove Illinois 60515
Iowa Methodist Medical Center Des Moines Iowa 50309
Massachusetts General Hospital Boston Massachusetts 02114
St. John's Mercy Medical Center St Louis Missouri 63141
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756
Albany Medical Center Albany New York 12208
Sisters of Charity Hospital Buffalo New York 14214
NYU Hospitals Center New York New York 10016
Mount Sinai School of Medicine New York New York 10029
Mission Hospitals Asheville North Carolina 28801
Mid Carolina Presbyterian Hospital Charlotte North Carolina 28204
Lindner Clinical Trial Center Cincinnati Ohio 45219
Cleveland Clinic Cleveland Ohio 44195
Jobst Vascular Center Toledo Ohio 43606
University of Pennsylvania Hospital Philadelphia Pennsylvania 19104
Allegheny General Hospital Pittsburgh Pennsylvania 15212
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232
Sanford Research Sioux Falls South Dakota 57104
Baptist Memorial Hospital Memphis Memphis Tennessee 38120
Premier Surgical Associates Powell Tennessee 37849
UT Southwestern Medical Center Dallas Texas 75390
Scott & White Memorial Medical Center Temple Texas 76508
Harborview Medical Center Seattle Washington 98104

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 NCT00705718, 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 Nov 2, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00705718 live on ClinicalTrials.gov.

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