A Trial of Skin Care Protocols for Facial Resurfacing
Completed · Phase 4
Conditions studied: Facial Photo Damage, Periocular Fine Wrinkles, Perioral Fine Wrinkles
In brief
The aims of the Skin Product Assessment Research study were to (1) develop an infrastructure and process for industry-sponsored, Plastic Surgery Educational Foundation (PSEF) research in facial aesthetic surgery and (2) test the research process by comparing outcomes of the Obagi Nu-Derm System (ODNS) and conventional therapy as treatment adjuncts in ablative facial resurfacing.
Key facts
- Study ID
- NCT01113606
- Run by
- The Plastic Surgery Foundation
- Last updated by the study team
- 2010-04-30
Who can join
Age: 18 and older, up to 65. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- patients with moderate to severe photo damage and rhytids, undergoing full or partial face resurfacing with chemical peel or ablative laser.
- Fitzpatrick I-IV skin types
You may not qualify if…
- patients unable to complete the regimen or who had used topical prescription steroids, retinoids, depigmentation products or other products containing hydroquinone and polyhydroxy acids within 8 weeks of enrollment.
Where it is running
- Suite 135 — Oxnard, California, United States
- Suite 175 — Rancho Santa Margarita, California, United States
- Aesthetic and Plastic Surgery Institute — Greeley, Colorado, United States
- Brevard Plastic Surgery and Skin Institute — Melbourne, Florida, United States
- Kentucky Aesthetic and Plastic Surgery Institute — Louisville, Kentucky, United States
- Center for Plastic and Reconstructive Surgery — Ypsilanti, Michigan, United States
- Body Aesthetic Plastic Surgery — St Louis, Missouri, United States
- Study site — New York, New York, United States
- Advanced Cosmetis Surgery — Greenville, South Carolina, United States
Full record on ClinicalTrials.gov
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