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Clinical Trial Summary

This prospective pivotal study is a double arm, randomized multi-center study evaluating the safety and performance of the MicroStent peripheral vascular stent system for use in arterial lesions below the knee. A total of 177 subjects will be enrolled at up to 25 centers and followed for up to 3 years, with the primary safety and efficacy endpoints evaluated 30 days and 6 months, respectively, post-implant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04025008
Study type Interventional
Source Micro Medical Solution, Inc.
Contact Kate Mandall
Phone (949) 292-5466
Email kmandall@micromedicalsolutions.net
Status Not yet recruiting
Phase N/A
Start date October 2019
Completion date August 2021

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