SELUTION4SFA Trial

Status Recruiting

Clinical Trial Summary

This study aims to demonstrate the safety and efficacy of the SELUTION SLR™ 018 DEB compared to plain (uncoated) balloon angioplasty in the treatment of peripheral arterial disease (PAD) in the superficial femoral artery (SFA) and proximal popliteal artery (PPA).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Peripheral Arterial Disease
Peripheral Vascular Diseases
Superficial Femoral Artery Stenosis

Clinical Trial Details

NCT number	NCT05132361
Study type	Interventional
Source	M.A. Med Alliance S.A.
Contact	Anna Hubert
Phone	+1(630)7294530
Email	anna.hubert@cordis.com
Status	Recruiting
Phase	N/A
Start date	December 1, 2022
Completion date	December 1, 2029

View Details

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