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Assessment of the Evolution of Wound Biomarkers in Venous Leg Ulcers Treated With KLOX Biophotonic System

Venous Leg Ulcer Clinical Trial

Official title:
A Prospective Controlled Randomized Clinical Study Exploring The Evolution Of Wound Biomarkers With TWO Dispensing Schedules Of The KLOX LumiHeal Gel And The KT-L Lamp Versus Standard Of Care In Venous Leg Ulcers

Clinical Trial Summary

The main purpose of the study is to evaluate the effect of KLOX BioPhotonic System (composed of KLOX LumiHeal Gel and KT-L Lamp) on the expression of wound biomarkers in the treatment of venous leg ulcers (VLU). Patients will be randomized in three groups, two different dispensing schedules of KLOX BioPhotonic System in addition to Standard of Care (SOC) will be used, and SOC alone.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03593369
Study type Interventional
Source KLOX Technologies Inc.
Contact Stephane Fauverghe, MD
Phone 450-680-4389
Email sfauverghe@kloxtechnologies.com
Status Recruiting
Phase N/A
Start date July 9, 2018
Completion date June 2020
View Details
See also
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