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Clinical Trial Summary

A total of at least 15 and up to 17 healthy subjects at a single site, aged 25-45 years old, who wish to receive a lifting effect and improved muscle definition, will be included in the study. The procedure will include treatments with the Legend Pro™ DMA™ technology. Photos will be obtained at pre-defined time points throughout the study.


Clinical Trial Description

Single center, prospective, open Label with Before & After Study Design. This study is designed to evaluate the immediate efficacy and safety of Legend Pro™'s DMA™ muscle stimulation technology. Treatment areas will include the face, buttocks, or abdominal region. Each subject will receive 1 treatment with no follow-up visits required. Interim assessment will be held after half of the study population has received treatment. The study population will be divided into three arms as follows: - 5 female subjects will receive treatment in the face area - 5 female subjects will receive treatment in the buttocks area - 5 male subjects will receive treatment in the abdominal region ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04296201
Study type Interventional
Source Lumenis Ltd.
Contact
Status Completed
Phase N/A
Start date September 1, 2020
Completion date February 15, 2021

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