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Clinical Trial Summary

The purpose of this trial is to assess the safety and efficacy of MDT-2113 for the interventional treatment of de novo and non-stented restenotic lesions in the superficial femoral artery (SFA) and the proximal popliteal artery (PPA) as compared to treatment with standard percutaneous transluminal angioplasty (PTA).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01947478
Study type Interventional
Source Medtronic Endovascular
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date April 2018

See also
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