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Clinical Trials/JPRN-UMIN000042417
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.

Registry
who.int
Start Date
November 13, 2021
End Date
March 23, 2021
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
IMEQRD Co., Ltd

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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