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Thoraflex Hybrid and Relay Extension Post-Approval Study — EXTEND  

Aortic Aneurysm Clinical Trial

Official title:
Thoraflex Hybrid and Relay Extension Post-Approval Study

Clinical Trial Summary

The goal of this observational study is to evaluate the Thoraflex Hybrid device alone and in combination with the RelayPro NBS stent-graft in the treatment of aortic disease affecting the aortic arch and descending aorta with or without involvement of the ascending aorta. Patients who undergo treatment with the Thoraflex Hybrid device with or without extension with a RelayPro NBS stent-graft will be eligible for enrolment and study activities and follow-up regime will follow standard care at each participating site. Participant involvement in the study will last for a total of 10 years from the point at which the Thoraflex Hybrid device is placed.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05639400
Study type Observational
Source Vascutek Ltd.
Contact Donna McDougall
Phone +441418125555
Email d.mcdougall@terumoaortic.com
Status Recruiting
Phase
Start date March 17, 2023
Completion date December 2036
View Details
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