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European Aortic Data Collection Project

NCT05896397 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2025-07-08

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and performance of Cook's various Custom-Made Stent-graft Devices (CMD) used for endovascular treatment of the aorta and related diseases by collecting information on the real-world use of the devices.

The study results will be used to support the continuation of the CMDs on the market. In addition, the study will support the manufacturers obligation for post market product surveillance as well as Cook's technology development.

Conditions

  • Complex Abdominal Aortic Aneurysm
  • Thoracoabdominal Aortic Aneurysm
  • Aortic Arch Aneurysm
  • Chronic Aortic Dissection

Interventions

PROCEDURE

Endovascular Aortic Treatments

Use of Cook's custom-made endovascular grafts to treat complex abdominal, thoracoabdominal aortic diseases, or aortic arch diseases such as aneurysms and dissections.

Sponsors & Collaborators

  • Cook Research Incorporated

    lead INDUSTRY

Principal Investigators

  • Stephan Haulon, MD,PhD · Hopital Marie Lannelongue

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-31
Primary Completion
2027-01-31
Completion
2030-12-31

Countries

  • Denmark
  • France
  • Germany
  • Italy
  • Sweden
  • 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 NCT05896397 on ClinicalTrials.gov