Treatment of the Face and Neck With Lower Ulthera System Energy Settings

Completed · Not applicable

Conditions studied: Skin Laxity

In brief

Up to 60 subjects will be enrolled. Enrolled subjects will receive one Ulthera® treatment on the face and neck. 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

NCT01713998

Run by

Ulthera, Inc

People needed

47

Starts

2011-09-01

Expected to finish

2012-10-01

Last updated by the study team

2017-12-11

Who can join

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

You may qualify if…

• Male or female, age 30 to 65 years.
• Subject in good health.
• Skin laxity on the face and neck

You may not qualify if…

• Presence of an active systemic or local skin disease that may affect wound healing.
• Severe solar elastosis.
• Excessive subcutaneous fat in the face or neck.
• Excessive skin laxity on the face or neck.
• Significant scarring in areas to be treated.
• Open wounds or lesions in the area to be treated.
• Severe or cystic acne on the area to be treated.

Where it is running

• Ulthera, Inc. — Mesa, Arizona, United States

Full record on ClinicalTrials.gov

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