Healthy Adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Japanese men and women aged 20 to 80 at the time of acquiring consent 2) Those who judged that a principal Investigator will meet this trial aim 3) Those who can take the test supplement for 3 months 4) If the subject are doing diet therapy or exercise therapy, those who do not change during the trial duration 5) Those who obtains written consent
Exclusion criteria
Exclusion criteria: 1)Those who suffering from severe cerebrovascular disease, heart disease, liver disease, renal disease, gastrointestinal disease, infection requiring notification 2)Those who suspected of suffering from acute infection such as influenza 3)who are receiving treatment for autoimmune diseases, chronic inflammatory diseases, allergic diseases 4)Those who received vaccination within 12 weeks before ingestion, or those who wish to consume during the test period 5)Those who with a history of major operations in the digestive system such as gastrectomy, gastrointestinal suture, intestinal resection 6)Those who with significant changes in physical condition before and after menopause 7)Those who with significant abnormalities in blood pressure measurement and blood test 8)Those who with advanced anemia 9)Those who are likely to have allergic symptoms to drugs or foods(especially mushrooms, soybeans, wheat) 10)Those who take chinese herbs, health foods, supplements(mushrooms, seaweeds, nucleic acids, Yeast, lactic acid bacteria, etc)and a medice that affect immune function, regularly. The subject will be able to take these kinds of things, if a principal investigator will permit those items. the subject should write it down in detail on the subject diary. 11)Those who are extremely irregular in excessive smoking and alcohol consumers, and lifestyle habits such as meals and sleep 12)Those who donate 400 ml blood within 12 weeks, 200 ml blood within 4 weeks or ingredient donation within 2 weeks 13)Those who are pregnant, nursing or who want pregnancy during the exam 14)Those who are participating in other clinical trials, or participating within 1 month 15)Those who are judged unqualified as a subject by a principal investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS(visual analogue scale)of any symptoms of cold and tiredness. | — |
Countries
Japan
Contacts
AKIYAMA SANGYO Co.,Ltd. Special Sales Division