JPRN-UMIN000041933
Completed
未知
Exploratory trial of bodily sensation evaluation by test-food intake - Exploratory trial of bodily sensation evaluation by test-food intake
CPCC Company Limited0 sites50 target enrollmentOctober 1, 2021
ConditionsHealthy female subjects
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy female subjects
- Sponsor
- CPCC Company Limited
- Enrollment
- 50
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\) Subjects with some kind of medical treatment continuously. 2\) Subjects taking steadily in the medicine and/or health\-specific/functional/health foods, which might affect the test results. 3\) Subjects who have been determined as a patient with the chronic fatigue syndrome (CFS), or subjects with severe fatigue just like the idiopathic chronic fatigue, judging from the principal/sub investigator's opinions. 4\) Subjects with some kind of medical treatment continuously. 5\) Subjects with atopic dermatitis, contact dermatitis and/or skin hypersensitivity. 6\) Subjects with excessive suntan, and/or some kind of work/sport outside for a long time. 7\) Subjects with some kind of specific care outside, and/or planning to receive the care during this trial. 8\) Pregnant, possibly pregnant, or lactating women. 9\) Subjects who have previous and/or current medical history of serious diseases in heart, liver, kidney and/or digestive organs. 10\) Subjects with excessive alcohol intake. 11\) Subjects with extremely irregular life rhythms, midnight work and/or irregular shift one. 12\) Subjects with previous medical history of drug and/or food allergy. 13\) Subjects who are now under the other clinical tests with some kind of medicines/foods, or took part in those tests within four weeks after this trial. 14\) Others who have been determined as ineligible for participation, according to the principal/sub investigator's opinions.
Outcomes
Primary Outcomes
Not specified
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