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Clinical Trial Summary

The clinical trial evaluates the clinical outcomes associated with the non-invasive treatment to obtain lift and tightening of the cheek tissue and improve jawline definition and submental skin laxity utilizing the Ulthera™ System which delivers ultrasound energy in a focused manner below the surface of the skin


Clinical Trial Description

The primary objective of this study is to demonstrate the effectiveness of the Ulthera™ System for the non-invasive dermatological treatment to obtain lift and tighten the cheek tissue.

The secondary objective of this study is to demonstrate the effectiveness of the Ulthera™ System for the non-invasive dermatological treatment for improvement in jawline definition and submental skin laxity at 3 and 6 months compared to baseline based on the consensus of the three masked reviewers. ;


Study Design


Related Conditions & MeSH terms

  • Cutis Laxa
  • Mild to Moderate Skin Laxity on Cheek
  • Mild to Moderate Skin Laxity on Upper Neck
  • Mild to Moderate Subcutaneous Fat on Cheek
  • Mild to Moderate Subcutaneous Fat on Upper Neck

NCT number NCT01368835
Study type Interventional
Source Merz North America, Inc.
Contact
Status Completed
Phase N/A
Start date July 2010
Completion date April 2011