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Aorfix Intelliflex First in Human Study — FIH-NZ  

Aortic Aneurysm, Abdominal Clinical Trial

Official title:
Aorfix™ Generation IV Delivery System "IntelliFlex™" Study

Clinical Trial Summary

The First In Human (FIH) study is a long-term, single center, non-randomized study established by Lombard Medical, Inc. to collect "on-label" data in the clinical setting on patients undergoing endovascular repair with IntelliFlex™, the latest generation of the Aorfix™ AAA Flexible Stent Graft Delivery System, for treatment of abdominal aortic and aorto-iliac aneurysms in anatomy where the aorta in the aneurysm neck is bent through an angle between 0° and 90°.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02907762
Study type Observational [Patient Registry]
Source Lombard Medical
Contact
Status Active, not recruiting
Phase
Start date November 2015
Completion date November 2021
View Details
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