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Clinical Trial Summary

An evaluation of the safety and performance of the STANZA Drug-eluting Resorbable Scaffold (DRS) system for the treatment of patients with obstructive superficial femoral artery disease.


Clinical Trial Description

The STANZA DRS system is comprised of a controlled release paclitaxel-eluting bioresorbable scaffold and a delivery system used in the treatment of superficial femoral artery disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02097082
Study type Interventional
Source Lyra Therapeutics
Contact
Status Completed
Phase N/A
Start date October 2013
Completion date May 2017

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