Verification study on the effects of test food intake on skin quality
- Conditions
- Healthy subjects
- Registration Number
- JPRN-UMIN000052867
- Lead Sponsor
- M&I Science CORP.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 200
Not provided
1.Subjects who regularly use the foods rich (yogurt, lactobacillus drinks, cheese, kimchi, pickles, etc.) in lactic acid bacteria, health foods and medicines at least 3 times a week. 2.Subjects who are currently receiving medication or outpatient treatment for some serious disease. 3.Subjects who are currently undergoing exercise or diet therapy under the supervision of a physician. 4.Subjects who may develop allergies to the test food. 5.Subjects who have a current or a history of drug dependence or alcohol dependence. 6.Subjects who are hospitalized for mental disorders (depression, etc.) or sleep disorders (insomnia, sleep apnea, etc.), or have a history of mental disorders in the past. 7.Subjects who have irregular rhythm of life due to night work or shift work. 8.Subjects who are with extremely irregular eating, sleeping, or other habits. 9.Subjects who have an extremely unbalanced diet. 10.Subjects who have or have had serious diseases such as brain diseases, malignant tumors, immune diseases, diabetes, liver diseases (hepatitis), kidney diseases, heart diseases, etc., thyroid diseases, adrenal diseases, and other metabolic diseases. 11.Subjects who have any experience with cosmetic procedures that affect the subject area. 12.Subjects who have skin diseases (atopic dermatitis, contact dermatitis, etc.), traumatic injuries, or who have subjective symptoms such as pain that may affect the examination. 13.Subjects who use health foods, dietary supplements, and medicines that affect the study. 14.Subjects who used beauty devices or beauty equipment within 1 month prior to the date of obtaining consent. 15.Subjects who have participated in other clinical trials (research) within 3 months retrospectively from the date of obtaining consent, or those who have plans to participate in other clinical trials (research) during the study period.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method