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Clinical Trial Summary

Several studies have suggested that the endogenous electric field and its polarity stimulate the proliferation and migration of epithelial cells and therefore promote wound healing. WoundEL® will reproduce the endogenous electrical current to stimulate all the factors contributing to healing. Electrostimulation of wounds, including the WoundEL® device, is a therapy listed but not yet reimbursed in France. The aim of this study is to show that the WoundEL® electrostimulation device is superior to the reference treatments recognized by the HAS.


Clinical Trial Description

Patients with a leg ulcer will be randomized to the "usual treatment" or "WoundEL" group. The progress of the leg ulcer will be monitored every 2 weeks for 8 weeks or sooner if wound healing occurs. All leg ulcers will be examined at 10 weeks to check for healing or the condition of the leg ulcer if it has not healed. A third-blind party will also assess the ulcer condition at 10 weeks, based on standardized photographs. The consumption of analgesics, pain and quality of life will be compared in the 2 groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04980898
Study type Interventional
Source CEN Biotech
Contact Arnaud TERRILLON-SEYTRE
Phone +330380682093
Email arnaud.terrillonseytre@groupecen.com
Status Recruiting
Phase N/A
Start date March 16, 2021
Completion date December 31, 2024

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