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Clinical Trial Summary

Clinical Study to Evaluate the Performance of the Profound System for the Treatment of Cellulite.


Clinical Trial Description

Up to 60 healthy female volunteers, seeking cellulite treatment, 18 to 60 years of age from up to 3 investigational sites.

Prospective, open-label, baseline-controlled, two arms, randomized, clinical study to evaluate the Profound device using the Dermal and SubQ Cartridges for minimally-invasive treatment of the upper thighs and buttocks cellulite appearance.

The treatment areas of the study subjects will be divided into two arms:

1. Arm 1 - the upper thigh/buttock on the left or right side of the body will undergo a single Profound treatment utilizing the Dermal and SubQ Cartridges

2. Arm 2 - the contralateral upper thigh/buttock side of the body will undergo a single Profound treatment utilizing the SubQ Cartridge only.

Methodology described in protocol to evaluate efficacy of treatments will be carried out at each visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03078647
Study type Interventional
Source Syneron Medical
Contact
Status Completed
Phase N/A
Start date September 13, 2017
Completion date January 31, 2019

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