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Clinical Trial Summary

1. Demonstrate superiority of treatment with the Ulthera DeepSEE System compared to untreated control for the improvement of skin laxity of the lower face and submental area. 2. Demonstrate the safety of treatment with the Ulthera DeepSEE System for the improvement of skin laxity of the lower face and submental area.


Clinical Trial Description

Subjects in the study received a single treatment with Ulthera DeepSEE system on the midface, lower face, submental (under the chin) and upper neck area using 3 DeepSEE (DS) transducers (DS 10-1.5, DS 7-3.0, DS 7-4.5) at either Day 1 or Day 90. Subjects treated at Day 1 were followed for 180 days after treatment and subjects treated at Day 90 were followed for 90 days after treatment. ;


Study Design


Related Conditions & MeSH terms

  • Cutis Laxa
  • Improvement in Skin Laxity of the Lower Face and Submentum

NCT number NCT04795622
Study type Interventional
Source Merz North America, Inc.
Contact
Status Completed
Phase N/A
Start date March 16, 2021
Completion date May 17, 2022