NCT01708434

Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees

Feasibility Study: Evaluation of the Ulthera® System for Lifting and Tightening of the Knees

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 30 (actual)
• Sponsor: Ulthera, Inc · Industry
• Sex: Female
• Age: 30 Years – 65 Years
• Healthy volunteers: Accepted

Summary

Enrolled subjects will receive one bilateral Ulthera® treatment on the knees. Up to 30 subjects will be enrolled. Study photos will be obtained prior to study treatment, immediately following study treatment, and at each post-treatment follow-up visit. Follow-up visits will occur at 90 and 180 days post-treatment.

Detailed description

This pilot study is a prospective, single-center clinical trial of the Ulthera® System for treating skin laxity on the knees. Global Aesthetic Improvement Scale scores and Patient Satisfaction questionnaires will be obtained at each follow-up visit.

Conditions

• Skin Laxity

Interventions

Type	Name	Description
DEVICE	Ulthera® System	Focused ultrasound energy delivered below the surface of the skin

Timeline

• Start date: 2011-06-01
• Primary completion: 2012-05-01
• Completion: 2012-08-01
• First posted: 2012-10-17
• Last updated: 2017-11-24

Locations

1 site across 1 country: United States