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Active, not recruiting Not applicable Interventional

Study of the Relay Pro® Thoracic Stent-Graft in Subjects With Traumatic Injury of the Descending Thoracic Aorta

ClinicalTrials.gov ID: NCT03090230

Public ClinicalTrials.gov record NCT03090230. 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, 6:47 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 Prospective, Multicenter, Non-Blinded, Non-Randomized Study of the RelayPro Thoracic Stent-Graft in Subjects With Traumatic Injury of the Descending Thoracic Aorta

Study identification

NCT ID
NCT03090230
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bolton Medical
Industry
Enrollment
50 participants

Conditions and interventions

Interventions

  • Relay Pro Thoracic 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
Apr 16, 2017
Primary completion
Dec 21, 2020
Completion
Nov 21, 2025
Last update posted
May 30, 2025

2017 – 2025

United States locations

U.S. sites
16
U.S. states
15
U.S. cities
16
Facility City State ZIP Site status
University of California, Irvine Irvine California 92868
Stanford Medicine Stanford California 94305-5639
Yale School of Medicine New Haven Connecticut 06510
Grady Memorial Hospital Atlanta Georgia 30303
Indiana University Health Indianapolis Indiana 46202
University of Iowa Hospital and Clinic Iowa City Iowa 52242
University of Maryland Medical Center Baltimore Maryland 21201
Beth Israel Deaconess Medical Center / Harvard Medical School Boston Massachusetts 02215
St. Louis University St Louis Missouri 63110
Atrium Health Charlotte North Carolina 28203
University Hospitals Cleveland Ohio 44106
University of Pennsylvania Medical Center / Penn Presbyterian Philadelphia Pennsylvania 19104
Vanderbilt University Medical Center Nashville Tennessee 37232
University of Virginia Charlottesville Virginia 22908
University of Washington Seattle Washington 98105
Medical College of Wisconsin 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03090230, 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 May 30, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03090230 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →