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Clinical Trial Summary

The aim of the study is to assess the safety and efficacy of the paclitaxelreleasing balloon catheter SeQuent® Please P to treat de novo and restenotic lesions in the superficial femoral artery and the proximal two segments of the popliteal artery with reference diameters ≥ 4mm & ≤ 7mm and lesion lengths ≥ 4 cm & ≤ 27 cm. It is the intention of this trial to treat suitable target lesions with DCB only.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01970579
Study type Interventional
Source B. Braun Melsungen AG
Contact
Status Completed
Phase Phase 3
Start date October 2013
Completion date December 2019

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