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Clinical Trial Summary

The objective of this study is to document the performance and the safety of UrgoStart Plus® Border, UrgoStart Plus® Pad and UrgoStart Interface® in the local treatment of diabetic foot ulcers (neuropathic or neuroischemic - non-critical ischemia) and venous or mixed predominantly venous leg ulcers, in real life conditions and current practice, in France.


Clinical Trial Description

This is an observational, non-interventional, prospective multicenter study, carried out in real-life conditions on CE marked medical devices used for their intended purpose. The study will be carried out in France, in accordance with national and European regulations (RDM 2017/745). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06135987
Study type Observational
Source Laboratoires URGO
Contact Anne SAUVADET, PhD
Phone +33380442884
Email a.sauvadet@fr.urgo.com
Status Recruiting
Phase
Start date June 24, 2022
Completion date October 2024

See also
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