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โ† Trials
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European Aortic Data Collection Project

Recruitingn/aAges any - anyAllCook Research Incorporated
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1\. Patients who will be treated with a Cook CMD Exclusion Criteria: 1. Patients who declare they are unable to complete clinical follow-up visit at the time of enrollment, or 2. 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.
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What it tests

  • Endovascular Aortic Treatments
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Where

18 sites
Aarhus University Hospital
Aarhus, Denmark
Rigshospitalet
Copenhagen, Denmark
Hopital Marie Lannelongue
Le Plessis-Robinson, France
CHU de Lille
Lille, France
University Hospital Hamburg Eppendorf
Hamburg, Germany
LMU Klinikum Munich
Munich, Germany
St. Franzikus-Hospital Munster
Mรผnster, Germany
Klinnikum Nurnberg
Nuremberg, Germany

โ€ฆand 10 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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