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Clinical Trial Summary

The purpose of this single site clinical study is to evaluate the safety and effectiveness of the Soliton Rapid Acoustic Pulse (RAP) device for the improvement of cellulite comparing two different RAP treatment doses.


Clinical Trial Description

This is a non-significant risk, single-center, prospective trial for safety, and efficacy using Soliton's RAP device for the improvement in the appearance of cellulite performed at 1 (one) clinical research site in the United States. Approximately 15 healthy female participants between the age of 18-55 inclusive will be enrolled in this study. Participants who sign the informed consent form and meet all the eligible criteria will be enrolled in the study. Each participant will undergo acoustic rapid pulse (RAP) treatments on each of the participants buttocks and legs. The participant's right buttock and leg will receive 100 Hz doses, and the participants left buttock and leg will receive 50 Hz doses. Total study duration is anticipated to be at or less than 55 weeks from the first participant visit to the last participant observation visit. A total of 3 visits, plus two optional visits are planned for this study as listed below: - Visit 1: Baseline/Screening (-30 Days to Day 0) - Visit 2: Treatment (Day 0) - Visit 3: 12-week Follow-Up Visit (+/- 14 Days) - Visit 4: 26-week Follow-Up Visit (+/- 14 Days) (Optional) - Visit 5: 52 Week Follow-Up Visit (+/- 14 Days) (Optional) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05199506
Study type Interventional
Source Soliton
Contact
Status Active, not recruiting
Phase N/A
Start date May 4, 2021
Completion date July 2022

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