Examination of the effects induced by research-food intakes continuously on immune parameters.
- Conditions
- Healthy male/female adults
- Registration Number
- JPRN-UMIN000046959
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 140
Not provided
Subjects - - (1) who take steadily (not less than 3 times a week) in the health-specific/functional/supplementary/health foods (e.g., immune function). (2) with excessive alcohol intake. (3) who will be under a large variable condition, such as house-moving, transfer, diet. (4) with extremely irregular eating habits / life rhythm (irregular shift work or midnight one). (5) with history of tonsil/appendix removal. (6) who have received affecting surgeries (colonoscopy, gallstones/gall bladder removal, gastric bypass) within half a year before the consent. (7) with any difficulty in giving up taking medicines (e.g., antibiotics, steroids, antihistamines) during this research. (8) who have taken antibiotics within the last month before beginning the research-food intakes, or will take those. (9) having continuous allergy, and will take medicine. (10) undergoing dental treatment for gingivitis/periodontitis, or bleeding daily in the mouth. (11) with heavy exercises, not less than 4 days a week. (12) being under other clinical researches, or participated in those within the last four weeks before this research, or will join those after the consent. (13) will vaccinate within the designated periods. (14) whose roomer/acquaintance will take part in this research. (15) with medical history of serious diseases in heart, liver, kidney or digestive organs. (16) with pregnant, possibly pregnant, or lactating. (17) having drug/food allergy. (18) donated their blood components and/or whole blood (0.2 L) within a month to this research. (19) donated his whole blood (0.4 L) within the last 3 months to this research. (20) donated her whole blood (0.4 L) within the last 4 months to this research. (21) being collected in total of his blood (1.2 L) within the last 12 months and in this research. (22) being collected in total of her blood (0.8 L) within the last 12 months and in this research. (23) determined as ineligible for participation, by the principal/sub investigator - -.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The analysis of the immune cell
- Secondary Outcome Measures
Name Time Method The antibody test of the saliva