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A study on effect of salt-marinated rice malt (shio koji) on fasting blood glucose level : A randomized, double blinded, placebo controlled study

A study on effect of salt-marinated rice malt (shio koji) on fasting blood glucose level : A randomized, double blinded, placebo controlled study - A study effect of salt-marinated rice malt (shio koji)on fasting blood glucose level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028238
Enrollment
48
Registered
2018-11-03
Start date
2017-07-15
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

Healthy adults

Interventions

intake of salt-marinated rice malt (shio koji) for 12 consecutive weeks intake of a placebo for 12 consecutive weeks

Sponsors

TTC Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males and females from 20 to 69 years of age (2)Fasting blood glucose level are ranged from 100 mg/dL to 125 mg/dL

Exclusion criteria

Exclusion criteria: (1)Subjects who routinely takes foods or medicines affecting the test result (2)Subjects who have a disease requiring regular medication or a history of serious diseases for which medication was required (3)Subjects who has under treatment or a history of serious disease (e.g., diabetes, or liver disease, kidney disease, or heart disease) (4)Heavy smoker, Heavy drinker (5)Subjects who is employed on a pre-dawn shift or on night duty more than 2 times (6)Subjects having possibilities for emerging allergy related to the study. (7)BMI is less than 18.5 or more than 30.0 (8)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (9)Subjects who have donated over 400 mL of blood and/or blood components within the last three months prior to the current study (10)Subjects who have participated in other clinical study within the last one month prior to the current study (11)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (12)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (13)Subjects judged as unsuitable for the study by the investigator for other reasons

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose level

Secondary

MeasureTime frame
HOMA-R ,HbA1c

Countries

Japan

Contacts

Public ContactChiharu Goto

TTC Co., Ltd. Clinical Research Planning Department

c.goto@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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