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Clinical Trials/JPRN-UMIN000033947
JPRN-UMIN000033947
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 sites75 target enrollmentSeptember 3, 2019
Conditionsot applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
ot applicable
Sponsor
CPCC Company Limited
Enrollment
75
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 3, 2019
End Date
December 19, 2018
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Subjects who (1\)consume yogurt over 3 days a week. (2\)consume lactic acid bacteria beverages and/or bifidobacterium beverages over 3 days a week. (3\)consume health food which have intestinal action. (4\)consume supplements include lactic bacteria, bifidobacterium and/or yeast over 3 days a week. (5\)consume vitamin supplements over 3 days a week. (6\)regularly use gastrointestinal agonist and/or female hormone. (7\)repeat constipation and diarrhea. (8\)defecate under 2 times in a week. (9\)defecate over 10 times in a week. (10\)have taken antibiotics within a month (11\)are being treated uterine and/or that medical historie. (12\)are pregnant or are lactating. (13\)have allergy to medicine and/or food. (14\)are atopic dermatitis, contact dermatitis and/or skin hypersensitivity. (15\)Subjects who have birthmark, scar and/or acne on the part of measurement. (16\)have severe past and/or current medical history in heart, liver, kidney and/or digestive organs. (17\)are heavy drinkers of alcohol. (18\)have excess irregular life rhythm such as shift work or midnight work. (19\)are currently being treated or who plan to be treated for pollen allergy. (20\)have rough skin because of pollen allergy. (21\)have excess suntan and/or who stay outside long time. (22\)are receiving special care of face and/or arm in the service. (23\)plan to go traveling abroad and/or to go swimming in the sea during this test period. (24\)are participating, have participated within 4 weeks and/or who plan to participate after informed consent of this test, in clinical test of other medicine or health food. (25\)donated over 200mL blood and/or blood components within a month. (26\)donated over 400mL blood within the last 4 months. (27\)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. (28\)Others they have been determined ineligible by principal investigator or sub\-investigator.

Outcomes

Primary Outcomes

Not specified

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