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Clinical Trial Summary

This is a prospective, multi-center, single-arm, non-blinded study designed to investigate the safety and efficacy of the Tack Endovascular System in subjects with post-balloon angioplasty (post-PTA) dissection(s) type(s) A through F in the superficial femoral and proximal popliteal arteries ranging in diameter from 2.5mm to 6.0mm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02522884
Study type Interventional
Source Philips Clinical & Medical Affairs Global
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date March 2020

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