Up to 30 subjects will be enrolled. Enrolled subjects will receive an Ulthera® treatment to one side of the body, treating the lateral buttock region. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained pre-treatment, immediately post-treatment, and at each follow-up visit.
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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
31
Focused ultrasound energy delivered below the surface of the skin.
Skin Laser and Surgery Specialist of New York and New Jersey
New York, New York, United States
Overall lifting and tightening of the buttocks and thighs.
As determined by a masked, qualitative assessment of photographs at three months post-treatment compared to baseline.
Time frame: 90 days post-treatment
Overall aesthetic improvement.
As determined by GAIS completed by the Investigator and subject.
Time frame: 90 and 180 days post-treatment.
Overall subject satisfaction.
As determined by subjects' completion of a Patient Satisfaction Questionnaire.
Time frame: 90 and 180 days post-treatment
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