Study of effect of blood pressure suppression by intake of Mekabu
Not Applicable
- Conditions
- Healthy Adults
- Registration Number
- JPRN-UMIN000046597
- Lead Sponsor
- Healthcare Systems Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1.Persons who have a chronic disease and is under medication, or has a serious disease history 2.Persons who are allergic to the test food 3.Persons who regularly take large amounts of the test food 4.Persons who regularly use medicines, specified insurance foods, health foods 5.Persons who have a history of hypertension treatment 6.Persons who participated in other examination during the first month before the start of the exam, or those who plan to participate in other exams following this exam 7.Persons who are judged inappropriate for the exam by the principal investigator 8.Persons who are pregnant, planning or hoping to be pregnant during the study period, or breastfeeding
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure (systolic blood pressure, diastolic blood pressure) at the beginning of the test or after the intake for 4 weeks.
- Secondary Outcome Measures
Name Time Method Salt intake, physical examination (body height, weight, BMI) and questionnaire on swelling (VAS) at the beginning of the test or after the intake for 4 weeks.