A Retrospective Study to Evaluate the Effectiveness of the Ulthera System

Completed

Conditions studied: Skin Laxity, Wrinkles

In brief

Up to 120 subjects within the study site's practice who have already had an Ultherapy™ treatment to the face and neck will be enrolled to monitor treatment effectiveness. Follow-up visits will occur at 90 and 180 days post-treatment. Study images will be obtained at each follow-up visit.

Key facts

Study ID

NCT01519934

Run by

Ulthera, Inc

People needed

48

Starts

2011-10-01

Expected to finish

2012-08-01

Last updated by the study team

2017-12-18

Who can join

Age: 25 and older, up to 85. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Male or female, age 25-85 years.
• Subject in good health.
• Received Ultherapy™ treatment prior to or on October 1, 2011, and must have had pre-treatment baseline photographs taken.
• Willingness and ability to comply with protocol requirements, including returning for follow-up visits.
• Absence of physical or psychological conditions unacceptable to the investigator.

You may not qualify if…

• Presence of an active systemic or local skin disease that may affect wound healing.
• Significant scarring in areas treated.
• Open wounds or lesions in the areas treated.
• Severe or cystic acne on the areas treated.
• Inability to understand the protocol or to give informed consent.

Where it is running

• Dermatology Cosmetic Laser Associates — San Diego, California, United States

Full record on ClinicalTrials.gov

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