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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040882
Enrollment
16
Registered
2021-06-28
Start date
2020-06-29
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy male adults

Interventions

Ingestion of the test food-A to the subjects, two packages a day (at breakfast and dinner) for 35 days. Ingestion of the test food-A to the subjects, two packages a day (at breakfast and dinner) for 2

Sponsors

CPCC Company Limited
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Healthy male subjects ranging in age from 40 to 60. (2) Subjects who gave informed consent to participate in this trial after being provided with an explanation of the protocol detail.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Immunostimulation effects

Secondary

MeasureTime frame
1. Thrombogenesis-inhibitory effects 2. Inhibitory effects of blood-glucose level 3. Normalization effects of cholesterol level 4. Safety assessment

Countries

Japan

Contacts

Public ContactMasanori Numa

CPCC Company Limited Planning & Sales Department

cpcc-contact@cpcc.co.jp03-5297-3112

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026