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Clinical Trial Summary

This is a prospective, randomized, multi-center, single-blind study to demonstrate the safety and effectiveness of the CVI Paclitaxel-coated percutaneous transluminal angioplasty (PTA) balloon versus bare PTA balloon for the treatment of patients with de novo occluded/stenotic or reoccluded/restenotic lesions of the superficial femoral (SFA) and popliteal arteries.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01858363
Study type Interventional
Source Spectranetics Corporation
Contact
Status Completed
Phase N/A
Start date November 2012
Completion date October 2020

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