Clinical Evaluation of a 1060 nm Diode Laser, PEMF and Vacuum Assisted MP RF for Non-invasive Fat Reduction

NACompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

September 19, 2019

Primary Completion Date

October 22, 2022

Study Completion Date

October 22, 2022

Conditions
Adipose Tissue Atrophy
Interventions
DEVICE

Venus Bliss

The FDA cleared device (Venus Bliss™) is a non-invasive medical aesthetic device designed for body contouring. The device is comprised of a console, four 1060 nm diode laser applicators (60 mm x 60 mm). A belt is included to allow the operator to secure the laser applicators on the lipolysis treatment area, allowing hands free operation. The device uses vacuum assisted radiofrequency (RF) and PEMF (pulsed electromagnetic field) technology which has been shown in clinical studies to be safe and effective in body circumferential reduction and skin tightening.

Trial Locations (5)

60026

aFresh Medispa, Chicago

75390

UT Southwestern Medical Center Department of Plastic Surgery, Dallas

90404

Batra Dermatology, Santa Monica

94022

Berman Skin Institute, Los Altos

95816

Laser & Skin Surgery Medical Group, Inc, Sacramento

All Listed Sponsors
lead

Venus Concept

INDUSTRY

NCT04012814 - Clinical Evaluation of a 1060 nm Diode Laser, PEMF and Vacuum Assisted MP RF for Non-invasive Fat Reduction | Biotech Hunter | Biotech Hunter