None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) A person who has consented to participate in this study and signed a written consent form. 2) Adults aged 35 to under 60 years old. 3) Those who have dry skin (Cornometer®CM825 measured moisture content index of 49 or less), have begun to produce wrinkles around their eyes, or have already produced them (visual evaluation grade 3 or more)
Exclusion criteria
Exclusion criteria: 1) A person who has skin abnormalities such as moles, acne, erythema, and capillary dilatation at the test spot 2) A person who is currently suffering from or undergoing treatment for skin diseases such as atopic dermatitis, psoriasis 3) A person who takes oral contraceptives, hormones, diuretics, and immunologic agents 4) A person who has taken an oral drug containing steroids or retinoids or has used an external application to the skin containing the relevant ingredients within three months of the first visit. 5) A person who has used functional cosmetics for wrinkle improvement or highly moisturizing cosmetics within two weeks of the first visit 6) A person who has undergone skin peeling, laser, chemical peeling, or other skin care procedures on the face within one month of the first visit, or Botox or fillers on the face within six months of the first visit 7) A person with the following diseases: uncontrolled hypertension or hypotension, uncontrolled diabetic, Renal dysfunction, Liver dysfunction, Mental illness such as schizophrenia, depression, drug addiction, alcoholism, A person who is hospitalized, receiving medication and undergoing rehabilitation due to skin diseases, asthma, heart diseases, central neurological disorders, etc. 8) A person who has continuously consumed herbal medicine, health functional foods and products containing relevant ingredients within one month of the first visit. 9) A smoker or a person who has quit smoking for not more than one year 10) A person who participated in other clinical study within one month of the first visit or who plan to participate in other clinical trials during this clinical study 11) Pregnant women or lactating women, and the person who plans to conceive during this clinical study 12) A person who has a hypersensitivity to ingredients contained in test and control foods or has experienced a severe food allergy reaction 13) A person who is deemed to be inappropriate to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| moisture amount of skin, skin moisturizing, Amount of dead skin cells, skin texture, skin elasticity, wrinkles around the eyes;Overall improvement | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical pathology test(blood, urine);vital signs;adverse event | — |
Countries
Korea, Republic of
Contacts
Yonsei University Health System, Severance Hospital