A study to evaluate the effect of fasting blood glucose level by ingestion of botanical ingredient-containing foods in adult males and females with a higher fasting blood glucose.

A study to evaluate the effect of fasting blood glucose level by ingestion of botanical ingredient-containing foods in adult males and females with a higher fasting blood glucose. - A study to evaluate the effect of fasting blood glucose level by ingestion of botanical ingredient-containing foods.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000032770

Enrollment

Registered

2019-10-03

Start date

2018-05-31

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

Interventions

Ingestion of botanical ingredient-containing food for 12 consecutive weeks. Intake of a placebo for 12 consecutive weeks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1)Males and females from 20 to 64 years of age (2)Fasting blood glucose level are ranged from 90 mg/dL to less than 126 mg/dL

Exclusion criteria

Exclusion criteria: (1)Subjects who eat botanical ingredient-containing food 3 times per week. (2)Subjects who routinely take foods or medicines affecting the test result (3)Subjects who have a disease requiring regular medication 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, or liver disease, kidney disease, or heart disease) (5)Subjects having possibilities for emerging allergy related to the study. (6)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (7)Subjects who have participated in other clinical study within the last one month prior to the current study (8)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (9)Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. (10)Subjects who are judged unfit to enroll in this trial by the investigator.

Design outcomes

Primary

Measure	Time frame
Fasting blood glucose level	—

Secondary

Measure	Time frame
HbA1c,Insulin	—

Countries

Japan

Contacts

Public ContactEri Yamazaki

TTC Co.,Ltd Clinical Research Planning Department

e.yamazaki@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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