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A study of safety and effect of miso on blood pressure in subjects with normal to mild hypertension

A study of safety and effect of miso on blood pressure in subjects with normal to mild hypertension - A study of safety and effect of miso on blood pressure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031764
Enrollment
40
Registered
2019-08-07
Start date
2018-03-19
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

2 test food A per day for 8 weeks 2 test food B per day for 8 weeks

Sponsors

TTC Co.,Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males and females aged 40 to less than 70 years old. (2) Those who falling under any of the following criteria. 130<=SBP<160 and/or 85<=DBP<100

Exclusion criteria

Exclusion criteria: (1) As a principle, 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

MeasureTime frame
Blood pressure

Countries

Japan

Contacts

Public ContactShingo Yamamichi

TTC Co.,Ltd Clinical Research Planning Department

s.yamamichi@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026