The purpose of this interventional study is to evaluate the effectiveness and safety of a hydrating gel containing aqua, carrageenan, polyvinyl pyrrolidone, algin, gellan gum, and hyaluronic acid. The study will assess the gel's ability to support optimal skin recovery following fractional CO₂ laser therapy and its effectiveness and safety as a daily adjunctive skincare treatment. Outcomes related to skin hydration, skin barrier function, tolerability, and adverse events will be evaluated throughout the study period. Female participants aged 18 to 60 years who provide informed consent will be enrolled in this study. Participants will undergo a 2-week priming period with topical tretinoin prior to fractional CO₂ laser treatment. Clinical evaluations will be performed at baseline, immediately after the laser procedure, and on Days 3, 7, and 14 post-treatment. Assessments conducted by a board-certified dermatologist will include dermoscopy, TEWAmeter assessment, erythema assessment, and evaluation of pain and discomfort using a Visual Analog Scale (VAS).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
51
Fractional CO₂ laser treatment performed according to the study protocol by a qualified dermatologist.
Hydrating gel containing aqua, carrageenan, polyvinyl pyrrolidone, algin, gellan gum, and hyaluronic acid.
Placebo gel matched in appearance and application method to the investigational hydrating gel.
Universitas Indonesia Hospital
Depok, West Java, Indonesia
Skin Hydration
Skin hydration will be evaluated by measuring skin capacitance using a corneometer.
Time frame: Baseline, immediately after treatment, Day 3, Day 7, and Day 14.
Dermoscopic Assessment of Skin Recovery
Dermoscopic evaluation of post-treatment skin changes and recovery.
Time frame: Baseline, immediately after treatment, Day 3, Day 7, and Day 14.
Erythema severity
Change in erythema severity assessed by dermatologist evaluation.
Time frame: Baseline, immediately after treatment, Day 3, Day 7, and Day 14.
Subjective assessment
Anamnesis, VAS (Visual Analog Scale) Score
Time frame: Baseline, Immediately after treatment, Day 3, Day 7, and Day 14.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.