Feasibility Study: Ulthera Treatment of the Buttocks and Thighs

This is a prospective, single-center, pilot clinical trial to evaluate the efficacy of the
Ulthera® System to improve buttock and thigh skin laxity. Global Aesthetic Improvement Scale
scores and patient satisfaction questionnaires will be obtained.

Inclusion Criteria:

- Male or female, age 30 to 65 years.

- Subject in good health.

- Skin laxity in the buttocks and thighs.

- Understands and accepts the obligation not to undergo any other procedures in the
areas to be treated and/or weight loss through the follow-up period.

- Willingness and ability to comply with protocol requirements, including returning for
follow-up visits and abstaining from exclusionary procedures for the duration of the
study.

- Subjects of childbearing potential must have a negative urine pregnancy test result
and must not be lactating at Visit 1 and be willing and able to use an acceptable
method of birth control (e.g., barrier methods used with a spermicidal agent, hormonal
methods, IUD, surgical sterilization, abstinence) during the study. Women will not be
considered of childbearing potential if one of the following conditions is documented
on the medical history: a) Postmenopausal for at least 12 months prior to study; b)
Without a uterus and/or both ovaries; or c) A bilateral tubal ligation at least six
months prior to study enrollment.

Exclusion Criteria:

- Presence of an active systemic or local skin disease that may affect wound healing.

- BMI equal to or greater than 40.

- Excessive subcutaneous fat in the buttocks and thighs.

- Excessive skin laxity in the buttocks and thighs.

- Significant weight fluctuation (±10 lbs) in the past 6 months.

- Taking weight-loss medications/supplements.

- Surgical or non-surgical treatments to the target areas in the last 12 months, e.g.,
liposuction.

- Inability to understand the protocol or to give informed consent.