None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Adults aged between 20 and 60 years with sensitive skin - Subjects who voluntarily signed the informed consent form after fully understanding the purpose and procedures of the study - Healthy subjects without acute or chronic diseases including skin disorders - Subjects who were available for follow-up during the study period
Exclusion criteria
Exclusion criteria: - Subjects who did not wish to participate or did not sign the informed consent form - Pregnant or breastfeeding women, or those planning pregnancy within 6 months - Subjects who had used topical steroids for more than one month for treatment of skin diseases - Subjects with abnormal skin conditions such as moles, acne, erythema, or telangiectasia at the test site - Subjects who had used cosmetics or drugs with similar efficacy on the test site within 3 months before the study - Subjects who had undergone dermatological procedures on the test site within 6 months before the study - Subjects with mental illness or cognitive impairment - Subjects considered unsuitable for participation by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Human Skin Primary Irritation Evaluation on Sensitive Skin | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of Adverse Skin Reactions | — |
Countries
Korea, Republic of
Contacts
SKINMED