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Clinical Trials/JPRN-UMIN000040882
JPRN-UMIN000040882
Completed
未知

Exploratory trial of clinical effects by ingestion of beta-glucan-containing test-food - Exploratory trial of clinical effects by ingestion of beta-glucan-containing test-food

CPCC Company Limited0 sites16 target enrollmentJune 28, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
CPCC Company Limited
Enrollment
16
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 28, 2021
End Date
August 3, 2020
Last Updated
2 years ago
Study Type
Interventional
Sex
Male

Investigators

Sponsor
CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Subjects with their body temperature of not less than 37\.5 degree centigrade at the first coming to clinic. (2\) Subjects with any symptoms just like the common cold within two weeks before the first coming to clinic. (3\) Subjects with some kind of medical treatment. (4\) Subjects who have regularly took in health\-specific / functional / health foods, containing a lot of beta\-glucan, over three times a week. (5\) Subjects who have regularly took in immunostimulation foods, over three times a week. (6\) Subjects with previous medical history of drug and/or food allergy. (7\) Subjects who are now under the other clinical tests with some kind of medicines/foods, or participated those tests within four weeks after the current trial. (8\) Subjects who donated over 200 mL of their whole blood and/or blood components within a month to the current trial. (9\) Subjects who donated over 400 mL of their whole blood within the last three months to the current trial. (10\) Subjects who are going to be collected over 1200 mL in total of their blood within the last twelve months, after adding the planned sampling blood amounts in this trial. (11\) Others who have been determined as ineligible for participation, judging from the principal/sub investigator's opinions.

Outcomes

Primary Outcomes

Not specified

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