Healthy Adults
Conditions
Interventions
Intake 200g of yogurt together with 2 tablespoons of ground sesame for 4 weeks.
Intake 200g of yogurt for 4 weeks.
none
Sponsors
Akasaka Family Clinic
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Persons who received a sufficient explanation of the purpose and contents of the study, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document 2.Male and Female who are 30 years old or more and under 60 years old 3.Persons who have troubles of eye and nasal discomfort. 4.Persons who can come to the designated day and be inspected.
Exclusion criteria
Exclusion criteria: 1.Persons who have any disease and are judged to have necessary treatment by the principal investigator. 2.Persons who are taken or applied medications for the treatment in the last one month. (excluding medicine used for needed basis such as headache, menstrual cramps and colds, etc.) 3.Persons with medical history with visceral disease and blood disease. 4.Persons who are judged to have diseases by the principal investigator and result of blood test or self-report. 5.Persons with self-report of medical history within last 6 months. 6.Persons who have severe anemia. 7.Persons who have an addiction to alcohol or a mental disease. 8.Persons who are a smoker or has been smoking for within last 10 years. 9.Persons who may cause allergic symptoms to test foods. 10.Persons who received hormone replacement therapy in the past 6 months. 11.Persons who were hospitalized and received treatment in the past 6 months. 12.Persons whose life style will change during the study period. 13.Persons who plan to intake new health functional foods and supplement foods during the study period. 14.Persons who participates in other clinical studies or participated in the last 3 months or plan to participate in other clinical studies. 15.Persons who are pregnant, planning or hoping to be pregnant during the study period, currently lactating. 16.Persons who were judged as inappropriate for subjects by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| QOL score Specific IgE (36 items) at the beginning of Interventional and after 4weeks of Interventional. | — |
Secondary
| Measure | Time frame |
|---|---|
| Th1/Th2 rate Intestinal Flora Physical examination(body height, weight, BMI, lean body mass) at the beginning of Interventional and after 4weeks of Interventional | — |
Countries
Japan
Contacts
Public ContactEriko Watanabe
Healthcare Systems Co., Ltd. Research and Development Department
Outcome results
None listed