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Clinical Trial Summary

Prospective, baseline-controlled evaluation of the UltraShape Power device for non-invasive fat reduction in flanks.


Clinical Trial Description

Eligible subjects will receive 3 bi-weekly treatments (2 weeks interval) with the UltraShape Power device according to the study protocol.

One random flank will be treated with one pass or remained as a control (no treatment) while the second flank will be treated with multiple passes.

Subjects will return for up to 4 follow up visits: 4 weeks, 8 weeks, 12 weeks and (optional) 24 weeks following end of treatment/s.

Each subject will be enrolled for total expected study duration of up to 28 weeks.

After last follow up visit, subjects who wish will receive compensation treatments (up to 3) on the flank who received regular treatment (single pass) or remained as a control (no treatment). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03502473
Study type Interventional
Source Syneron Medical
Contact
Status Withdrawn
Phase N/A
Start date March 7, 2018
Completion date September 7, 2019

See also
  Status Clinical Trial Phase
Completed NCT02748928 - UltraShape Power for Abdominal Fat and Circumference Reduction N/A
Recruiting NCT02700152 - Clinical Study to Evaluate the Safety and Efficacy of the UltraShape Device for Non-Invasive Abdominal Fat Reduction N/A