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Data Registry Following Patients Using Supera Stent in the Femoral Arteries — STRONG  

Peripheral Artery Disease Clinical Trial

Official title:
Supera Treatment Registry Observing Neointimal Growth

Clinical Trial Summary

Long-term, observational, prospective, multicenter registry following patients who have been implanted with the SUPERA Interwoven Self-Expanding Nitinol Stent for treating stenosis in the superficial femoral and/or femoropopliteal arteries.

Clinical Trial Description

This registry follows up to 200 patients for at least 5 years.

The STRONG Data Registry will follow patients under real world conditions, evaluating restenosis rates, periprocedural/postprocedural complications, patency, target lesion revascularization, walking distance, stent fractures, and adverse events/serious adverse events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01154751
Study type Interventional
Source Abbott Vascular
Contact
Status Terminated
Phase N/A
Start date November 2008
Completion date August 2015
View Details
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