Study of the Effects of Ingestion of the Test Food on Skin Function and Intestinal Environment.
- Conditions
- o
- Registration Number
- JPRN-UMIN000053476
- Lead Sponsor
- TES Holdings Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 60
Not provided
1)Individuals using medical products. 2)Individuals with strange skin conditions at measurement points. 3)Individuals who have wounds or inflammation in the evaluation site. 4)Individuals who used a drug to treat a disease in the past 1 month. 5)Individuals who have a history of serious hepatopathy, kidney damage, heart disease and hematological disease. 6)Individuals who are a patient or have a history of or endocrine disease. 7)Individuals with serious anemia. 8)Individuals whose BMI is over 30 kg/m2. 9)Individuals who are sensitive to test product or other foods, and medical products. 10)Individuals who habitually take the foods for specified health uses (FOSHU) or functional food. 11)Individuals who have a habit to ingest or use health-promoting foods, or supplements containing similar composition with a test food in the past 3 months or will ingest those foods during the test period. 12)Individuals who excessively take alcohol. 13)Individuals who are patient or have a history of psychiatric disease. 14)Individuals who are a smoker. 15)Individuals who engage in work such as sales or delivery, and who spend long time in outdoor activities and exposure to ultraviolet rays in their daily lives. 16)Individuals who engage in a night work. 17)Individuals with possible changes of lifestyle during the test period. 18)Individuals who will develop seasonal allergy symptoms like hay fever and be to suffer from worsening eyes and nose symptoms or use anti-allergic drugs during the test period. 19)Individuals who neglect skin care. 20)Individuals who will get sunburned during the test period. 21)Individuals who had been conducted an operation or beauty treatment on the evaluation area within 6 months before the start of the test. 22)Individuals who are pregnant, lactating, or who may become pregnant during the test period. 23)Individuals who participated in other clinical studies in the past 3 months. 24)Individuals judged inappropriate for the study by the principal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method