JPRN-UMIN000037734
Completed
未知
A confirmation study for the improvement effect of skin quality by the test food consumption - A confirmation study for the improvement effect of skin quality by the test food consumption
CPCC Company Limited0 sites110 target enrollmentAugust 21, 2020
Conditionsot applicable
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- ot applicable
- Sponsor
- CPCC Company Limited
- Enrollment
- 110
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •Subjects who 1\)have habit to consume yogurt more than 3 days a week. 2\)have habit to consume beverages include lactic acid bacteria and/or bifidobacteria more than 2 days a week. 3\)have habit to consume vitamin supplements more than 3 days a week. 4\)regularly use gastrointestinal drugs or female hormone. 5\)have taken antibiotics within a month. 6\)are currently being treated or who plan to be treated for pollen allergy. 7\)repeat constipation and diarrhea. 8\)declared their defecate habit as \>\= 3 times and/or \<\= 9 times in a week. 9\)have severe past and/or current medical history. 10\)are being treated or have medical histories uterine fibroid and/or ovarian cyst. 11\)are pregnant or are lactating. 12\)have allergy to medicine and/or food. 13\)are atopic dermatitis, contact dermatitis and/or skin hypersensitivity. 14\)have rough skin because of pollen allergy. 15\)have birthmark, scar and/or acne on the part of measurement. 16\)have excess suntan and/or who stay outside long time. 17\)plan to go traveling abroad and/or to go swimming in the sea during this test period. 18\)are receiving special care of face and/or arm in the service. 19\)have excess irregular meal cycle and/or have irregular life rhythm. 20\)are excessive smoker and/or heavy drinkers of alcohol. 21\)are participating, who have participated within 4 weeks and/or who plan to participate after informed consent, in other clinical test. 22\)donated over 200mL blood and/or blood components within a month. 23\)donated over 400mL blood within the last 4 months. 24\)will be collected over 800mL blood and/or blood components when the sampling amounts within the last 12 months are adding to the planned sampling amounts of this study. 25\)Others they have been determined ineligible by investigator.
Outcomes
Primary Outcomes
Not specified
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