None (Healthy adults)
Conditions
Interventions
Microorganism-originated food, 1 portion of food per day for 4 weeks.
Placebo (not containing microorganism-originated food), 1 portion of food per day for 4 weeks.
Sponsors
Kirin Company, Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Males and females aged from 20 to less than 60 years old, when giving the informed consent. 2) Individuals work in daytime and do not have night shift. 3) Individuals who can avoid eating foods containing food originated from a microorganism 4) Individuals who give the informed consents in writing, after receiving enough explanation of the purpose and details of the study, understanding the study well, and deciding to attend the study with their own will. 5) Individuals who can accomplish their tasks in the study at the appointed date. 6) Individuals who are judged suitable for this study by the investigators.
Exclusion criteria
Exclusion criteria: 1) Individuals who can't avoid medication which effects on the results. 2) Individuals who can't avoid functional foods which effects on the results. 3) Individuals who are pregnant or willing to be pregnant. Individuals who are breast-feeding. 4) Individuals who are enrolled in other clinical trials. 5) Individuals who have a medical history of serious hepatopathy, nephropathy, or heart disease. 6) Individuals who have a medical history of viral hepatitis. 7) Individuals who have serious anemia. 8) Individuals who have serious hay fever symptoms and cannot avoid steroidal agents. 9) Individuals who are judged unsuitable for this study by the investigator for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Activities of immunocytes (Neutrophil phagoctytosis activities etc.) | — |
Countries
Japan
Contacts
Public ContactToshio Fujii
Kirin Company, Limited Research Laboratories for Health Science & Food Technologies
Outcome results
None listed