ClinicaliQ Trial Snapshot
- European Aortic Data Collection Project — Recruiting • Cardiology / Cardiovascular • NCT05896397.
- What is being tested: Safety and real-world performance of Cook's Custom-Made Stent-graft Devices (CMD) for endovascular aortic treatment across diverse aortic pathologies through prospective data collection.
- Patient eligibility overview: Adults with aortic disease requiring endovascular stent-graft intervention who are anatomically suitable for custom-made device implantation, as determined by treating clinicians across European centres.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
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.
Eligibility Snapshot
- : 1. Patients who will be treated with a Cook CMD
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.