A Human study to evaluate the effect on the skin health and safety of Vegetable Collagen(VC-H1)
- Conditions
- Not Applicable
- Registration Number
- KCT0009307
- Lead Sponsor
- Global Medical Research Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 100
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)
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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method moisture amount of skin, skin moisturizing, Amount of dead skin cells, skin texture, skin elasticity, wrinkles around the eyes;Overall improvement
- Secondary Outcome Measures
Name Time Method Clinical pathology test(blood, urine);vital signs;adverse event