CompletedNot Applicable

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

United States47 participantsStarted 2011-09

Plain-language summary

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.

Who can participate

Age range30 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male or female, age 30 to 65 years. * Subject in good health. * Skin laxity on the face and neck Exclusion Criteria: * 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.

What they're measuring

Subjects' Assessment of Pain During Treatment With Lower Energy Settings

Timeframe: Participants were assessed for the duration of study treatment, an average of 75 minutes

Overall Improvement in Skin Laxity on the Face and Neck

Timeframe: 90 days post-treatment

Trial details

NCT IDNCT01713998

SponsorUlthera, Inc

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2012-06

Results submitted2013-06-19

View on ClinicalTrials.gov More Skin Laxity trials