Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

Up to 30 subjects will be enrolled. Enrolled subjects will receive an Ulthera® treatment to one side of the body, treating the lateral buttock region. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.

Key facts

Study ID
NCT01708460
Run by
Ulthera, Inc
People needed
31
Starts
2011-12-01
Expected to finish
2013-07-01
Last updated by the study team
2017-11-24

Who can join

Age: 30 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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