None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Individuals who can follow the clinical trial procedures and adhere to the visit schedule. 2) Individuals who agree to discontinue all dermatological treatments, including facial lifting procedures, during the clinical trial period. 3) Individuals who voluntarily sign the consent form
Exclusion criteria
Exclusion criteria: 1) Women who are pregnant or breastfeeding and those who do not agree to the contraception methods specified in the protocol. 2) Individuals with lesions at the test site. 3) Individuals with allergies or hypersensitivity. 4) Individuals with inflammatory and/or infectious diseases on the face that may affect the clinical trial. 5) Individuals who have received systemic steroids or phototherapy within one month prior to participating in the clinical trial. 6) Individuals who have undergone or plan to undergo skin procedures (e.g., scaling, Botox, fillers, laser treatments, tattoos, etc.) within three months before or during the study period. 7) Individuals deemed unsuitable for the clinical trial by the principal investigator or study staff for any other reasons beyond the criteria listed above.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cheek/mouth area lifting;Skin volume;Skin pores;Skin hydration | — |
Secondary
| Measure | Time frame |
|---|---|
| Nasolabial folds/around the mouth wrinkles;Skin texture;skin elasticity;Skin density | — |
Countries
Korea, Republic of
Contacts
Yonsei University Health System, Severance Hospital