A study of excessive intake of the food containing plant-derived ingredient. (SME-2019-02-FOSHUS)
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000037518
- Lead Sponsor
- Suntory MONOZUKURI Expert Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 48
Not provided
(1) Subjects who are with treatment. (2) Subjects whose systolic pressure <90 mmHg. (3) Females in pregnancy,lactation and scheduled pregnancy period. (4) Subjects who donated over 200ml blood components or whole blood within 4 weeks. (5) Male Subjects who donated over 400ml whole blood within 12 weeks. (6) Female who donated over 400ml whole blood within 16 weeks. (7) Male subjects whose blood was collected more than 1200 mL within the last twelve months when the amount of blood sampling in the current study is added. (8) Female subjects whose blood was collected more than 800 mL within the last twelve months when the amount of blood sampling in the current study is added. (9) Subjects who are participating in other clinical studies, or who finished clinical study within 4 weeks. (10) Subjects who are; (a)With present heart disorder,liver disorder,or kidney disorder. (b)With history of cardiac disorder. (c)With diabetes mellitus. (d)With allergy to drugs or foods. (e)With glaucoma. (f)With hyponatremia. (11) Subjects who constantly use supplements and/or functional foods (including Food for Specified Health Uses) affecting the test results. (12) Subjects who drink alcohol or smoke a lot. (13) Subjects who have an extremely irregular diet habit or alternative work schedule or work on midnight shift. (14) Subjects who themselves or family living together work at a company that plans, researches, develops, manufactures or sells supplements and/or functional foods (including Food for Specified Health Uses). (15) Subjects who are deemed to be unsuitable by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method