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Clinical Trial Summary

The aim of the study is to assess the safety and efficacy of the Multi-LOC® peripheral stent system to treat de novo and restenotic lesions (no in-stent restenosis (ISR), no restenosis post drug coated balloon (DCB) after flow limiting plain old balloon angioplasty (POBA) and/or DCB dilatations in the superficial femoral artery (SFA) and popliteal segments (P1, P2 & P3)


Clinical Trial Description

This study is an non-randomized, prospective, multi-center, non-interventional study (registry, for Germany: §23b MPG) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02531230
Study type Observational
Source B. Braun Melsungen AG
Contact
Status Completed
Phase
Start date July 2015
Completion date August 2017

See also
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