GORE® EXCLUDER® Endoprosthesis French Mandatory Registry

Status Completed

Clinical Trial Summary

This is a French Registry mandated by the French National Health Authority assessing long-term (5-years) safety of the GORE® Excluder® Endoprosthesis in the treatment of infra-renal Abdominal Aortic Aneurysms (AAA).

Clinical Trial Description

The use of abdominal aortic endoprostheses makes the treatment of infra-renal abdominal aortic aneurysms possible, with implantation via the femoral artery, thus avoiding a very invasive surgical procedure. The French National Authority for Health requires a 5-year follow-up as part of the renewal for reimbursement for these endoprostheses. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02308839
Study type	Observational [Patient Registry]
Source	W.L.Gore & Associates
Contact
Status	Completed
Phase
Start date	July 2012
Completion date	October 5, 2018

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