None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Males and females aged 20 to less than 65 years old. (2) Those who falling under any of the following criteria. 1. 120<=SBP<130 and/or 80<=DBP<85 2. 130<=SBP<160 and/or 85<=DBP<90
Exclusion criteria
Exclusion criteria: (1) Subjects who constantly use oral medication and/or functional foods which may affecting blood pressure. (2) Subjects having possibilities for emerging allergy related to the study. (3) Subjects having a disease requiring treatment or a history of serious diseases for which medication was required. (4) Subjects who have under treatment or a history of serious disease (e.g., diabetes, liver disease, kidney disease, or heart disease). (5) Subjects who are judged as unsuitable for the current study based on the results of clinical and physical preliminary examination. (6) Subjects who are judged as unsuitable for the current study based on the results of lifestyle questionnaire (ex. Subjects who eat miso soup 4 times per week). (7) Subjects who cannot defend restrictions during the study period. (8) Subjects who have participated in other clinical studies within the last one month prior to the current study or are planned to participate in other studies after obtaining informed consent for the current study. (9) Subjects who have a lifestyle affect the result of this study (ex. work on midnight shift) or subjects who are going to change to a lifestyle affect the result of this study. (10) Subjects who intend to become pregnant or lactating. (11) Subjects judged as unsuitable for the current study by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure | — |
Countries
Japan
Contacts
TTC Co.,Ltd Clinical Research Planning Department