Safety and Effectiveness Evaluation of the Device in Achieving Submental Lift

NACompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

June 25, 2016

Primary Completion Date

February 20, 2017

Study Completion Date

April 8, 2017

Conditions
Skin Laxity
Interventions
DEVICE

Percutaneous Radiofrequency single treatment

Percutaneous Radiofrequency single treatment' under controlled temperature conditions based on pre-defined amounts of energy as controlled by the device internal algorithm, and investigator expertise. Additionally, Hunsted solution will be infused in the treatment area to eliminate the electrode/fiber to touch inner layers of the skin. External temperatures (skin surface) will be monitored using a temperature reading camera to ensure the external temperature stays within acceptable levels during the procedure Ice packs will also be used as needed to cool the treatment area based on the Thermal Camera Reading where the . heat delivery may be exceeding the threshold.

Trial Locations (1)

07042

New Jersey Plastic Surgery, Montclair

All Listed Sponsors
lead

ThermiGen, LLC

INDUSTRY

NCT02832674 - Safety and Effectiveness Evaluation of the Device in Achieving Submental Lift | Biotech Hunter | Biotech Hunter