JPRN-UMIN000042417
Completed
未知
The effect of continuous intake of test foods on health condition change - The effect of continuous intake of test foods on health condition change
IMEQRD Co., Ltd0 sites220 target enrollmentNovember 13, 2021
ConditionsHealthy adults
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy adults
- Sponsor
- IMEQRD Co., Ltd
- Enrollment
- 220
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\.Those who are currently under continuous treatment with drugs. 2\. Those who have a positive reaction in the infectious disease test. 3\. Those who are on a diet or exercise therapy under the supervision of a doctor. 4\. Those who have a current or history of serious illness. 5\. Those with atopic dermatitis, bronchial asthma, or chronic bronchitis 6\. Those who have hay fever and allergic rhinitis (including seasonal and perennial) 7\. Those who are currently using quasi\-drugs, foods for specified health uses, health foods and supplements. Those who can quit during the test period after obtaining consent are allowed to participate. 8\. Those who have been vaccinated against influenza vaccine after October 2020, or who are planning to be vaccinated during the test period 9\. Those who have a past and current medical history of drug or food allergy. 10\. Those who consume alcohol excessively (alcohol equivalent 60g or more / day) 11\. Those who have excessive smoking habits (21 or more cigarettes / day) 12\. Those who work in shifts, such as those who work night shifts 13\. Those who are planning to travel abroad during the test period 14\. Those who wish to become pregnant, breastfeeding, or during the test period 15\. Those who have participated in other clinical trials within one month before obtaining consent, or those who plan to participate during the trial period 16\. Those who are judged by the investigator or coordinator to be unsuitable for participating in this study
Outcomes
Primary Outcomes
Not specified
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