None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy male and female adults aged between 20 and 60 years 2. Individuals without active skin disease at the test site 3. Subjects who voluntarily provided written informed consent after receiving a full explanation of the study 4. Subjects able to comply with study procedures and visit schedule
Exclusion criteria
Exclusion criteria: 1. Individuals with skin disease, wounds, or inflammation at the test site 2. Individuals who received dermatological treatment or procedures within the last 3 months 3. Individuals with known hypersensitivity or allergic reactions to cosmetic ingredients 4. Pregnant or breastfeeding women 5. Individuals deemed unsuitable for participation by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of skin barrier function measured by reduction in transepidal water loss (TEWL) | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement of skin hydration (increase in surface and inner moisture);Improvement of skin texture (keratin condition);Reduction in pore area and pore volume;Improvement of redness induced by external physical stimuli | — |
Countries
Korea, Republic of
Contacts
SKINMED