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Clinical Trial Summary

This is a prospective, multicenter, single arm study designed to evaluate the safety and efficacy of the Temporary Bare Spur Stent System (Spur Stent System).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05358353
Study type Interventional
Source ReFlow Medical, Inc.
Contact Carolyn Mascho
Phone (616) 802-8575
Email cmascho@reflowmedical.com
Status Recruiting
Phase N/A
Start date October 1, 2022
Completion date October 22, 2024

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