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European Aortic Data Collection Project

Study acronym: EADC
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Site details revised at 6 of 18 sitesv7
  2. Study sites: 16 to 18
    • Primary completion date: Dec 2026 to Jan 2027
    v6
  3. Site details revised at 2 of 16 sitesv5
  4. Study sites: 8 to 16v4
  5. Study sites: 2 to 8v3
  6. Trial status: Not Yet Recruiting to Recruiting
    • Primary endpoints revised (2)
    • Start date changed from estimate of Jun 2023 to May 31, 2023
    • Site details revised at 2 of 2 sites
    v2
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05896397
Lead Sponsor Cook Research Incorporated
Conditions
(from sponsor)		 Complex Abdominal Aortic Aneurysm, Thoracoabdominal Aortic Aneurysm, Aortic Arch Aneurysm, Chronic Aortic Dissection
Related terms Aneurysm, Aortic Arch, Aortic Aneurysm, Aortic Aneurysm, Thoracoabdominal, Aortic Dissection
Enrollment 600 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov