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Feasibility Study: Evaluation of the Ulthera® System for Treatment of Abdominal Tissue

Skin Laxity Clinical Trial

Official title:
Feasibility Study: Evaluation of the Ulthera® System for Efficacious and Safe Treatment of Laxity/Crepiness and Texture of Abdominal Tissue

Clinical Trial Summary

Enrolled subjects will receive one UltherapyTM treatment on the abdomen. 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.

Clinical Trial Description

This is a prospective, single-center, pilot clinical trial to evaluate the efficacy of the Ulthera® System for improving laxity/crepiness and texture of abdominal tissue. Changes from baseline in the laxity, crepiness and texture of abdominal skin will be assessed at each study follow-up visit. Global Aesthetic Improvement Scale scores, assessments of dermal thickness, and patient satisfaction questionnaires will also be obtained. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01708499
Study type Interventional
Source Merz Pharmaceuticals, LLC
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date April 2013
View Details
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