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A study for verification of Immune index by intake test food-3

A study for verification of Immune index by intake test food-3 - A study for verification of Immune index by intake test food-3

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000038557
Enrollment
18
Registered
2020-04-01
Start date
2019-11-08
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 individuals

Interventions

None listed

Sponsors

Leverage Brain Inc. Clinical Trial Department
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Subjects of both sexes above 20 years old- under 64 years old. 2) Subjects who competent to consent and give voluntary consent in writing with full understanding after receiving explanation of this study aim and contents.

Exclusion criteria

Exclusion criteria: 1) Subjects who have serious disorders on hepatic, kidney, cardiac, lung, digestive organs, blood, endocrine system, metabolic system. 2) Subjects who are under medication (especially subject who take warfarin) on a steady basis or history of medication for serious disorders. 3) Subjects who are under treatment for digestive system and Immune system disease (Autoimmune diseases, etc.) that effects on this study, or have previous history, or have history of operation on digestive system. 4) Subjects who regularly intake food with health-promoting benefits function or supplements that may possibly effect on the immunity. 5) Subjects work irregular hours on the night shift or irregular shift. 6) Subjects who smoke excessively and drink alcohol regularly. 7) Subjects with irregular lifestyle habit such as diet meal and sleep. 8) Subjects who had made blood donation within 4 weeks. 9) Subjects with history of sensitivity to the ingredients of test food. 10) Pregnant, lactating women or willing to be pregnancy during the study. 11) Subjects who participated in other monitoring study within 1 month prior to obtaining informed consent. 12) Any candidates considered to be unsuitable for enrollment in the opinion of the principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Influenza vaccine antibody titer (Type A,Type B), and NK Cell activity

Secondary

MeasureTime frame
Triglycerides,totalcholesterol,HDL cholesterol,LDLcholesterol,The subject questionnaire regarding QOL

Countries

Japan

Contacts

Public Contactshigeru imai

Leverage Brain Inc. Clinical Trial Department

imai@levbrain.com08072900404

Outcome results

None listed

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