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Terumo Aortic Global Endovascular Registry

NCT04246463 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-03-13

No results posted yet for this 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.

Conditions

  • Abdominal Aortic Aneurysm
  • Thoracic Aortic Aneurysm
  • Surgery

Interventions

DEVICE

Thoracic

Implant of a Relay stent graft system

DEVICE

Abdominal

Implant with an Anaconda or Treo Stent graft system

DEVICE

Custom Device

Implant of a Fenestrated device such as Fenestrated Anaconda or Fenestrated TREO, Relay Branch or other customised device

DEVICE

Illiac Artery

Implant with an Anaconda Iliac leg only

Sponsors & Collaborators

  • Bolton Medical

    collaborator INDUSTRY

  • Vascutek Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-17
Primary Completion
2029-11-30
Completion
2030-11-30

Countries

  • United States
  • Belgium
  • France
  • Germany
  • Italy
  • Netherlands
  • Portugal
  • Spain
  • Switzerland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04246463 on ClinicalTrials.gov