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SIGNATURE Study : DCB (Legflow) vs POBA in Fempop Arteries — SIGNATURE  

Peripheral Arterial Disease Clinical Trial

Official title:
SIGNATURE Study: Post-market, Randomized Controlled, Multicenter, Single Blinded Prospective Trial Investigating the Paclitaxel-Coated Balloon (Legflow DCB) Treatment Versus Uncoated Balloon Angioplasty Treatment for Femoro-popliteal Lesions.

Clinical Trial Summary

The aim of this study is to demonstrate the superiority in safety and efficacy of the Legflow DCB vs standard uncoated POBA in a randomized controlled (RCT) for treatment of patients with symptomatic peripheral artery disease (PAD) due to stenosis, restenosis or occlusion of the femoral and/or popliteal arteries.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04971772
Study type Observational
Source Cardionovum GmbH
Contact Sabrina Overhagen, Dr.
Phone +4915780591411
Email info@fcre.eu
Status Recruiting
Phase
Start date June 8, 2022
Completion date May 2026
View Details
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