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Clinical Trial Summary

Up to 30 subjects will be enrolled. All subjects will receive one Ultherapy treatment to the lower two thirds of the face and neck. Subjects will be equally grouped into those with a history of submentoplasty and or rhytidectomy and those naive to submentoplasty and or rhytidectomy. Follow-up visits will occur at 14, 30, 60, 90 and 180 days following treatment. Study images will be obtained pre-treatment, 30-60 minutes post-treatment, and at each follow-up visit.


Clinical Trial Description

This is a prospective single center study. Subjects will be enrolled one per group as they present. Efficacy will be determined by the change in submental volume and cervicomental angle. GAIS and patient satisfaction questionnaires will also be obtained. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01708928
Study type Interventional
Source Merz Pharmaceuticals, LLC
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date August 2012

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