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Clinical Trial Summary

This is a non-randomized, prospective, single center pilot study designed to evaluate the safety of the Temporary Spur Stent System to treat patients with infrapopliteal arterial disease, when used in conjunction with a commercially available limus-base drug coated balloon.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04162418
Study type Interventional
Source ReFlow Medical, Inc.
Contact
Status Completed
Phase N/A
Start date February 14, 2020
Completion date September 30, 2023

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