Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees
| Status: | Completed |
|---|---|
| Conditions: | Dermatology |
| Therapuetic Areas: | Dermatology / Plastic Surgery |
| Healthy: | No |
| Age Range: | 30 - 65 |
| Updated: | 11/25/2017 |
| Start Date: | June 2011 |
| End Date: | August 2012 |
Feasibility Study: Evaluation of the Ulthera® System for Lifting and Tightening of the Knees
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.
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.
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.
treating skin laxity on the knees. Global Aesthetic Improvement Scale scores and Patient
Satisfaction questionnaires will be obtained at each follow-up visit.
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
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