Feasibility Study: Lifting and Tightening of the Elbows

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

Up to 20 subjects will be treated. Treated subjects will receive one Ulthera® treatment on the elbows. 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.

Key facts

Study ID

NCT01708382

Run by

Ulthera, Inc

People needed

21

Starts

2011-09-01

Expected to finish

2013-02-01

Last updated by the study team

2017-11-24

Who can join

Age: 21 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female, age 21 to 65 years.
• Subject in good health.
• Mild to moderate skin laxity on the elbows.
• Understands and accepts the obligation not to undergo any other procedures in the areas to be treated 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

You may not qualify if…

• Presence of an active systemic or local skin disease that may affect wound healing.
• Excessive subcutaneous fat around the elbows.
• Excessive skin laxity around the elbows.
• Significant scarring in areas to be treated.
• Significant open wounds or lesions in the area to be treated

Where it is running

• New York Cosmetic, Skin and Laser Surgery Center — New York, New York, United States

Full record on ClinicalTrials.gov

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