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Completed Not applicable Interventional Results available

Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating Patients Who Have a Blunt Thoracic Aortic Injury

ClinicalTrials.gov ID: NCT01092767

Public ClinicalTrials.gov record NCT01092767. 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 22, 2026, 12:45 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

Evaluation of the Clinical Performance of the Valiant Thoracic Stent Graft With the Captivia Delivery System for the Endovascular Treatment of Blunt Thoracic Aortic Injuries (RESCUE)

Study identification

NCT ID
NCT01092767
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Cardiovascular
Industry
Enrollment
50 participants

Conditions and interventions

Interventions

  • Valiant Thoracic Stent Graft with the Captivia Delivery 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
Mar 31, 2010
Primary completion
Mar 31, 2012
Completion
Apr 30, 2017
Last update posted
Oct 28, 2021

2010 – 2017

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294
Cedars Sinai Medical Center Los Angeles California 90048
Harbor UCLA Torrance California 90502
Denver Health Denver Colorado 80204
Yale New Haven Hospital New Haven Connecticut 06510
University of Florida Shands Hospital Gainesville Florida 32608
University of Miami Jackson Memorial Miami Florida 33136
Bayfront Medical Center St. Petersburg Florida 33709
Maine Medical Center Portland Maine 04105
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
University of Michigan Ann Arbor Michigan 48109
William Beaumont Hospital Royal Oak Michigan 48073
Cooper Health Camden New Jersey 08103
Vascular Research Institute Morristown New Jersey 07960
Duke University Medical Center Durham North Carolina 27710
Toledo Hospital / Jobst Vascular Center Toledo Ohio 43606
UT Southwestern Dallas Texas 75390
Memorial Hermann Heart and Vascular Institute Houston Texas 77030
Brooke Army Medical Center San Antonio Texas 78234
Scott and White Memorial Temple Texas 76508
University Of Virginia Charlottesville Virginia 22908
Sentara Norfolk General Vascular & Transplant Specialists Norfolk Virginia 23507
Medical College of Wisconsin Froedtert Hospital Milwaukee Wisconsin 53226

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01092767, 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 Oct 28, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01092767 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →