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ACTIVE NOT RECRUITING NA

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

NCT03090230 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to investigate the safety and effectiveness of the RelayPro Thoracic Stent-Grafts in subjects with traumatic injury of the descending thoracic aorta (DTA)

Interventions

  • DEVICE Relay Pro Thoracic Stent-Graft System

Study Locations (16)

California

  • University of California, Irvine — Irvine
  • Stanford Medicine — Stanford

Connecticut

  • Yale School of Medicine — New Haven

Georgia

  • Grady Memorial Hospital — Atlanta

Indiana

  • Indiana University Health — Indianapolis

Iowa

  • University of Iowa Hospital and Clinic — Iowa City

Maryland

  • University of Maryland Medical Center — Baltimore

Massachusetts

  • Beth Israel Deaconess Medical Center / Harvard Medical School — Boston

Missouri

  • St. Louis University — St Louis

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2017-04-17
Est. Completion 2025-11-22
Phase NA

Sponsor

Bolton Medical

36 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03090230

The ClinicalTrials.gov registry entry for NCT03090230 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bolton Medical, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Other Specified Injury of Thoracic Aorta appearing as the primary indexed condition, and to 1 intervention — of which Relay Pro Thoracic Stent-Graft System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03090230 reports 16 study locations spanning 15 distinct geographic areas — top geographies include California, Connecticut, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03090230 about?

NCT03090230 is a clinical study titled "Study of the Relay Pro® Thoracic Stent-Graft in Subjects With Traumatic Injury of the Descending Thoracic Aorta". The purpose of this study is to investigate the safety and effectiveness of the RelayPro Thoracic Stent-Grafts in subjects with traumatic injury of the descending thoracic aorta (DTA)

What is the current status of trial NCT03090230?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2017-04-17. Estimated completion is 2025-11-22.

What conditions does trial NCT03090230 study?

This clinical trial studies the following conditions: Other Specified Injury of Thoracic Aorta. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03090230?

The interventions under investigation include: Relay Pro Thoracic Stent-Graft System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03090230?

This trial is sponsored by Bolton Medical, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03090230 being conducted?

This trial has 16 study locations across California, Connecticut, Georgia, Indiana, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial