None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants who met all of the following criteria were eligible for inclusion in the study: 1. Male or female adults aged between 20 and 40 years 2. Individuals with acne-prone skin as assessed by the investigator 3. Individuals who voluntarily agreed to participate after receiving sufficient explanation of the study objectives and procedures 4. Individuals who were able to comply with the study visits and procedures throughout the study period
Exclusion criteria
Exclusion criteria: Participants meeting any of the following criteria were excluded from the study: 1. Individuals with severe skin diseases, infections, inflammation, or lesions at the test site 2. Individuals who had recently received dermatological treatments or procedures that could affect the study results 3. Individuals who required the use of other cosmetic or pharmaceutical products on the test area during the study period 4. Pregnant or breastfeeding women 5. Individuals deemed inappropriate for study participation by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in follicular and comedone formation after application of the test product | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of follicular and comedone ratios between the test product application site, non-application site, and comedogenic substance-applied site | — |
Countries
Korea, Republic of
Contacts
SKINMED