A Study on the Effect of Plant-Derived Products on skin functio
- Conditions
- o
- Registration Number
- JPRN-UMIN000043067
- Lead Sponsor
- TES Holdings Co., Ltd.
- Brief Summary
Statistically significant difference was confirmed in the primary outcome.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 50
Not provided
Subjects (who) 1)contract disease and are under treatment. 2)with skin disease, such as atopic dermatitis. 3)with strange skin conditions at measurement points. 4)used a drug to treat a disease in the past 1 month. 5)used antibiotics within the last 2 weeks prior to the screening and pre-intake test. 6)have a history of and/or contract serious diseases (eg, liver disease, kidney disease, heart disease, lung disease, blood disease). 7)have a history and/or contract digestive disease. 8)with serious anemia. 9)whose BMI are 30 or more. 10)have allergic reaction to ingredients of test foods and other foods or drugs. 11)have a habit to use drugs claiming to improve skin function in the past 3 months. 12)have a habit to use Foods with Function Claims, functional foods and/or supplements claiming to improve skin function in the past 3 months and/or are planning to use those foods during test periods. 13)have a habit to take foods related to green juice in the past 3 months and/or are planning to use those foods during test periods. 14)regularly take foods containing lactic acid bacteria, bifidobacteria, oligosaccharides, and/or viable bacteria. 15)are or are possibly pregnant, or are lactating. 16)have excessive alcohol intake more than 20 g/day of pure alcohol equivalent. 17)with psychiatric disease. 18)are smokers. 19)with possible changes of life style during test periods. 20)will develop seasonal allergy symptoms, such as pollinosis, eye and nose symptoms and/or use an anti-allergic drug. 21)neglect skin care. 22)can't avoid direct sunlight exposure, such as sunburn, during test periods. 23)had been conducted an operation or beauty treatment on the test spot in the past 6 months. 24)are participating and/or had participated in other clinical studies within the last 3 months. 25)are judged as unsuitable for the current study by the investigator for other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Skin moisture content
- Secondary Outcome Measures
Name Time Method Transepidermal water loss Skin viscoelasticity Observation for skin condition by dermatologists Questionnaire survey (Visual Analogue Scale) on the physical condition