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European Aortic Data Collection Project

This trial has no sites in United States.

It has sites in 6 countries. Choose a country to see its sites.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Cook Research Incorporated
Trial code
NCT05896397
Record updated
4 June 2026
Original description
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.Read full original descriptionShow less

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.

Inclusion: Patients who will be treated with a Cook CMD.

Exclusion: Patients who declare they are unable to complete clinical follow-up visit at the time of enrollment, or; Patients or his/her legally authorized representative objects to extraction of patient's data from the medical record, or unwilling to sign the Informed Consent.

ClinicalTrials.gov NCT05896397

Under construction, not live – European Aortic Data Collection Project (NCT05896397) – Frontlight Research