Evaluation of efficacy of electro-stimulation of the abdominal muscle and truSculpt ID for fat reduction and non-invasive body sculpting

    Not Recruiting
Updated on 12 January 2021


This is single-center, open-label, prospective study of the Cutera truSculpt Flex device to assess the efficacy of this device in improving muscle tone, and in furthering the improvement of body contouring results when paired with treatments with the Cutera truSculpt ID device, which aims to improve body contouring by targeting fat reduction. Enrolled subjects will be assigned to one of three possible treatment arms according to body type and investigator discretion.

Participants will either receive one truSculpt ID treatment, one truSculpt ID plus six truSculpt Flex treatments, or six truSculpt Flex treatments. Participants will also be asked to come in for follow-up visits at 8-weeks and/or 12-weeks following their last treatment to assess changes in abdominal circumference and muscle/fat composition. All services are provided at no cost.



  • Physical exam and assessments of study condition to be provided at no cost by an experienced provider.
  • No insurance necessary.
  • Compensation will be provided at the end of study participation.

Condition *Healthy Patient Studies
Clinical Study IdentifierTX219133
Last Modified on12 January 2021

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