A Retrospective Study to Evaluate the Effectiveness of the Ulthera System
| Status: | Completed |
|---|---|
| Conditions: | Cosmetic, Dermatology |
| Therapuetic Areas: | Dermatology / Plastic Surgery |
| Healthy: | No |
| Age Range: | 25 - 85 |
| Updated: | 12/20/2017 |
| Start Date: | October 2011 |
| End Date: | August 2012 |
Retrospective Evaluation of the Ulthera System for Lifting and Tightening of the Face and Neck
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.
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.
This is a retrospective, single-center clinical trial to evaluate the efficacy of the Ulthera
System for non-invasive treatment of skin texture and laxity six months after treatment.
Global Aesthetic Improvement Scale scores, patient satisfaction questionnaires, and quality
of life questionnaires will be obtained.
System for non-invasive treatment of skin texture and laxity six months after treatment.
Global Aesthetic Improvement Scale scores, patient satisfaction questionnaires, and quality
of life questionnaires will be obtained.
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
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