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Study identifier: NCT07222397 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

2910 nm Erbium-Doped Fluoride Fiber Glass Laser for the Treatment of Advanced Perioral Lines and Wrinkles

Condition: Photodamaged Skin · Rhytids · Lines Skin  ·  Sponsor: FA Corporation

PhaseNA
Planned participants20
Who can joinAll sexes, 50 Years to 80 Years
Healthy volunteersNo

About this study

The primary objective is to assess the efficacy, safety and satisfaction associated with the resurfacing treatment of perioral lines and wrinkles with the 2,910 nm mid-infrared Fiber Laser (UltraClear, Acclaro Medical) using both superficial epidermis ablation capabilities and the deep ablative and coagulative capabilities into the dermis for rejuvenation. Participants will receive up to two treatments spaced 6-8 weeks apart, followed by a 1-month and 3-month follow-up visit during which the device will be evaluated for its effectiveness defined as improvement addressing perioral lines and wrinkles utilizing multiple scales completed by the investigator and blinded Independent Photographic Reviewers (IPRs). Additionally, safety, subjective overall aesthetic improvement and satisfaction will be monitored and tracked.

This description comes directly from the study's public registry record.

Talk to the study team

Mary Dick, MD  ·  713-900-3900  ·  drdick@dermlasersurgery.com

Leah Dickerson  ·  leah@dermlasersurgery.com

Always discuss trial participation with your own doctor first.

Locations (1)

Dermatology & Laser Surgery CenterHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07222397