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Clinical Trial Summary

This study will evaluate the clinical efficacy and safety of the BTL-899 device for toning of buttocks. The study is a prospective multi-center open-label two-arm study. The subjects will be enrolled and assigned into two study groups. The subjects will be enrolled and assigned into two study groups; HIFEM+RF (HR) and HIFEM (H) group. Subjects of both groups will be required to complete four (4) treatment visits and two follow-up visits.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04871503
Study type Interventional
Source BTL Industries Ltd.
Contact
Status Completed
Phase N/A
Start date March 1, 2021
Completion date January 12, 2022

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