None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Healthy adults aged between 20 and 40 years with acne-prone skin - Subjects who voluntarily signed the informed consent form after fully understanding the purpose and procedures of the study - Subjects who were able to comply with the study protocol and visit schedule - Subjects whose facial skin condition was suitable for evaluation
Exclusion criteria
Exclusion criteria: - Subjects who did not agree to participate in the study - Pregnant or breastfeeding women, or those planning pregnancy during the study period - Subjects with severe skin disorders or abnormal skin conditions at the test site - Subjects who had used cosmetics or medications with similar efficacy within a specified period before the study - Subjects who had undergone dermatological procedures within a specified period before the study - Subjects considered unsuitable for participation by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pore Improvement Effect | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement of Transepidermal Water Loss (TEWL);Skin Soothing Effect;Skin Hydration Improvement Effect;Dark Spot Improvement Effect;Suitability for Acne-Prone Skin | — |
Countries
Korea, Republic of
Contacts
SKINMED