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RECRUITING

Terumo Aortic Global Endovascular Registry

NCT04246463 · View on ClinicalTrials.gov ↗

Study Summary

Multi-arm, multi-center, open label, prospective observational registry designed to obtain safety and performance data on the use of CE marked and custom Terumo Aortic endovascular grafts.

Interventions

  • DEVICE Thoracic
  • DEVICE Abdominal
  • DEVICE Custom Device
  • DEVICE Illiac Artery

Study Locations (20)

Other

  • Imeldaziekenhuis — Bonheiden
  • Clinques Uni. St Lucs — Brussels
  • Hôpital Pneumologique et Cardiovasculaire Louis-Pradel — Bron

Colorado

  • University of Colorado Anschutz Medical Campus — Aurora
  • UC Health Memorial Hospital Center — Colorado Springs

Pennsylvania

  • University of Pennsylvania — Philadelphia
  • University of Pittsburgh — Pittsburgh

Texas

  • Ascension Texas Cardiovascular / UT Dell Medical School — Austin
  • Baylor, Scott & White Health (BSW Health) — Texas City

Virginia

  • University of Virgina — Charlottesville
  • Sentara Heart Hospital — Norfolk

California

  • Long Beach Memorial Medical Center — Long Beach

Connecticut

  • Yale University — New Haven

District of Columbia

  • MedStar Washington Hospital Center — Washington D.C.

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2019-12-17
Est. Completion 2030-11

Sponsor

Vascutek

32 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04246463

The ClinicalTrials.gov registry entry for NCT04246463 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vascutek, which has 32 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 4 interventions — of which Thoracic 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: NCT04246463 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Other, Colorado, Pennsylvania. 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 NCT04246463 about?

NCT04246463 is a clinical study titled "Terumo Aortic Global Endovascular Registry". Multi-arm, multi-center, open label, prospective observational registry designed to obtain safety and performance data on the use of CE marked and custom Terumo Aortic endovascular grafts.

What is the current status of trial NCT04246463?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2019-12-17. Estimated completion is 2030-11.

What conditions does trial NCT04246463 study?

This clinical trial studies the following conditions: Surgery, Abdominal Aortic Aneurysm, Thoracic Aortic Aneurysm. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04246463?

The interventions under investigation include: Thoracic (DEVICE), Abdominal (DEVICE), Custom Device (DEVICE), Illiac Artery (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04246463?

This trial is sponsored by Vascutek, which has 32 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04246463 being conducted?

This trial has 20 study locations across California, Colorado, Connecticut, District of Columbia, Florida. 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