About this trial
Evaluate the effectiveness of topical hyaluronic acid, ascorbic acid, and sodium DNA following ablative fractional laser treatment in objectively reversing facial skin alterations induced by photoaging.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male and female subjects, over 30 years of age, with moderate skin changes associated with elasticity, wrinkles, roughness, pigmentation, erythema, and pore size; with at least 12 points on the SASSQ scale. Fitzpatrick skin type I-III. Participants who agree to take part in the protocol
Disqualifiers
Fitzpatrick skin type IV-VI. Local infections or inflammatory disorders.. Neoplasms suspected of being malignant. Allergy to hyaluronic acid, ascorbic acid, and sodium DNA. Hypersensitivity to fractional CO2 laser. Pregnancy or breastfeeding. Local or systemic adverse reaction
Trial design
Single group
Treatments tested in this trial
topical hyaluronic acid, ascorbic acid, and sodium DNA following ablative fractional laser treatment
DrugThe study involves the application of ascorbic acid, hyaluronic acid, and sodium DNA in preparation for their use following the administration of a fractional CO2 laser treatment
Treatment groups
Trial outcomes
Primary outcomes
Skin quality
Quantitative enhancement that can be assessed using a validated scale (SASSQ)
Sponsors and contacts
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