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Clinical Trial Summary

The purpose of the post-market study was to evaluate the safety and performance of the FUSION Vascular Graft.


Clinical Trial Description

This study was a prospective, single-arm, multicenter study conducted in Germany and Austria to evaluate the FUSION Vascular Graft in patients with peripheral arterial occlusive disease undergoing above-the-knee bypass. Follow-up visits were performed at 30 days, 6 months, 12 months and included patency and post operative complications not associated with bypass patency. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01601496
Study type Interventional
Source Maquet Cardiovascular
Contact
Status Terminated
Phase N/A
Start date October 26, 2009
Completion date July 24, 2013