Clinical Trial

Safety and Efficacy of 2910 nm Fiber Laser Resurfacing and Laser-Coring

Not Yet Recruiting
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Summary
The primary objective of this clinical trial is to evaluate the safety and effectiveness of the 2,910 nm mid-infrared erbium-doped fluoride fiber glass laser (UltraClear, Acclaro Medical) for non-invasive dermatological aesthetic treatment of three facial regions: eyebrow lift (Region 1), submental tissue lift (Region 2), and improvement of rhytids and skin laxity in the cheeks, midface, and jawline (Region 3).
Trial Details
NCT Number NCT07254884
Lead Sponsor FA Corporation
Conditions Rhytids, Skin Laxity
Enrollment 40 participants
Start Date 2025-11
Primary Completion 2026-11 (estimated)
Study Completion 2026-11 (estimated)
Updated on ClinicalTrials.gov 2025-11-28