Influence on reducing allergies reactions of eyes and nose by consumption of test foods
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000038255
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Not provided
1) Subjects who plan some treatment during test period. 2) Subjects who use oral steroid medicine in order to treatment allergy. 3) Subjects who regularly use and/or are not able to quit use medicines, quasi-drugs and herbal medicines those have the inhibition effects of allergy and concerned to give influence for test results. 4) Subjects who regularly use and/or are not able to quit use healthy foods those advocate to have the inhibition effects of allergy and concerned to give influence for test results. 5) Females who are pregnant or could become pregnant, and who are lactating. 6) Subjects who have previous and/or current medical history of serious disease 7) Subjects who use oral medicines and/or nasal drops those are antihistamine or anti-allergy 8) Subjects who don't intake test food and/or don't enter the Web diary against the instruction of administrator during test period. 9) Subjects who excessive alcohol intake. 10) Subjects who have non-allergic nasal inflammation 11) Subjects who can't eat lotus root 12) Subjects who have food allergy 13) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 14) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. 15) Males who donated over 400mL blood within the last three months to the current study. 16) Females who donated over 400mL blood within the last four months to the current study. 17) Males who will be collected over 1200mL blood, when the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 18) Females who will be collected over 800mL blood when, the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 19) Others who have been determined ineligible by principal investigator or sub-investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method