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

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

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.

Key facts

Study ID

NCT01708434

Run by

Ulthera, Inc

People needed

30

Starts

2011-06-01

Expected to finish

2012-08-01

Last updated by the study team

2017-11-24

Who can join

Age: 30 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female, aged 30 to 65 years.
• Subject in good health.
• Mild to moderate skin laxity around the knees.
• Understands and accepts the obligation not to undergo any other procedures in the areas to be treated through the follow-up period.

You may not qualify if…

• Presence of an active systemic or local skin disease that may affect wound healing.
• Excessive subcutaneous fat around the knees.
• Excessive skin laxity around the knees.

Where it is running

• Tennessee Clinical Research Center — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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