Fractional CO2 Laser-assisted Delivery of Hyaluronic Acid, Ascorbic Acid and Sodium DNA For Enhancing Facial Skin Quality in Individuals Over the Age of 30

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age30+
SponsorInstituto de Oftalmología Fundación Conde de Valenciana

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • topical hyaluronic acid, ascorbic acid, and sodium DNA following ablative fractional laser treatment

    Drug

    The 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

30 Participants
are divided into 1 treatment group
Group A: Application of ascorbic acid, hyaluronic acid, and sodium DNA in preparation for their use followingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Skin quality

Quantitative enhancement that can be assessed using a validated scale (SASSQ)

Time frame
From enrollment to the end of treatment at 4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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