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Clinical Trial Summary

Up to 15 subjects will be enrolled. Enrolled subjects will receive one Ulthera® treatment on the face and neck. Follow-up visits will occur at 45, 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.


Clinical Trial Description

This is a prospective, single-center, pilot clinical trial to evaluate the efficacy of the Ulthera® System to improve jawline definition and submental skin laxity. Changes from baseline in the Fitzpatrick Facial Wrinkle Scale and facial pigmentation will be assessed at study follow-up visits. Global Aesthetic Improvement Scale scores, patient satisfaction questionnaires, and quality of life questionnaires will be obtained. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01713907
Study type Interventional
Source Merz Pharmaceuticals, LLC
Contact
Status Terminated
Phase N/A
Start date June 2011
Completion date January 2012

See also
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