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Randomized, Controlled, Split-Face and Split-Neck study to evaluate Adjuvant Efficacy of Topical Antioxidant Combinations Following Microneedling and Microneedle radiofrequency

Randomized, Controlled, Split-Face and Split-Neck study to evaluate Adjuvant Efficacy of Topical Antioxidant Combinations Following Microneedling and Microneedle radiofrequency

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010443
Enrollment
33
Registered
2025-04-22
Start date
2024-05-02
Completion date
Unknown
Last updated
2025-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery, Others(antioxidant cosmetic) : This clinical study involves a total of 33 patients exhibiting phenotypes of skin aging such as pigmentation and wrinkles. The treatment will be appli

Sponsors

Yonsei University Yongin Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy male or female subjects between the ages of 30 and 65 who do not meet the exclusion criteria. 2) Individuals who clinically require skin improvement through laser treatment for conditions such as melasma, decreased elasticity, or wrinkles. 3) Subjects who are able to participate in follow-up visits during the clinical trial period. 4) Individuals who have been adequately informed about this clinical trial, can provide written consent at the screening visit, and can comply with the requirements of the clinical trial.

Exclusion criteria

Exclusion criteria: 1) Patients with infectious skin diseases. 2) Patients with a history of other skin diseases at the treatment site besides decreased elasticity, wrinkles, or pigmentation. 3) Patients with keloid disorder or diseases related to collagen and elastic fibers. 4) Patients with psychiatric problems. 5) Individuals at risk of bleeding during treatment due to anticoagulant medication. 6) Individuals allergic to local anesthetics (lidocaine). 7) Pregnant or breastfeeding women, and women who may be pregnant. 8) Individuals with acute or chronic diseases that may affect the study results. 9) Patients who have undergone filler or fat grafting surgery within the last 3 months. 10) Individuals who have used topical steroids for more than 2 weeks to treat skin conditions. 11) Individuals with a history of cosmetic laser treatment, chemical peels, or plastic surgery on the face within 6 months prior to screening. 12) Individuals deemed unsuitable for the clinical trial by the investigator's judgment. 13) Patients who cannot understand the purpose of this clinical trial or cannot comply with the required procedures for treatment and research.

Design outcomes

Primary

MeasureTime frame
Global Aesthetic Improvement Scale ;9-point Fitzpatrick Wrinkle and Elastosis Scale

Secondary

MeasureTime frame
Half-face modified Melasma Area and Severity Index (hemi-MASI);Modified graffith’s scale;Measuring Skin Pigmentation and Redness;Measurement of skin hydration;Measurement of skin elasticity;Subject skin improvement (satisfaction) survey evaluation;Investigator skin improvement survey evaluation;Assessment of collagen changes through skin tissue biopsy;Assessment of microbiome distribution changes

Countries

Korea, Republic of

Contacts

Public Contactjihee kim

Yonsei University Yongin Severance Hospital

mygirljihee@gmail.com+82-31-5189-8778

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026