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A study of intake of the test food on postprandial blood glucose level

A randomized, single-blind, crossover study to assess intake of the test food on postprandial blood glucose level - A study of intake of the test food on postprandial blood glucose level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049868
Enrollment
20
Registered
2023-02-01
Start date
2023-02-08
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 volunteer

Interventions

Single ingestion of SAC high containing food 1 and carbohydrate food Single ingestion of SAC high containing food 2 and carbohydrate food Single ingestion of SAC high containing food 3 and carbohydrat

Sponsors

Momoya Co., Ltd.
Lead Sponsor
Kagawa Nutrition University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy males and females aged 18 to less than 65 years old. 2) Subjects who are capable of understanding the study, and those who can give written informed consents.

Exclusion criteria

Exclusion criteria: 1) Subjects who are allergic to products related to the test material of this study. 2) Subjects who are addicted to alcohol or has an extremely irregular dietary habit. 3) Subjects who take drugs, quasi-drugs, dietary supplements, health foods or something other which possibly have effects on this study. 4) Subjects who are determined to have diabetes, are receiving or have previously received treatment, medication, or lifestyle guidance from a physician due to diabetes. 5) Subjects who are pregnant or breastfeeding, or desires to get pregnant during the study period. 6) Subjects who are judged unsuitable for this study by principal investigator.

Design outcomes

Primary

MeasureTime frame
Postprandial blood glucose level

Secondary

MeasureTime frame
Blood pressure VAS

Countries

Japan

Contacts

Public ContactYuko Nagata

Momoya Co., Ltd. Research & Development Division

y.nagata@momoya.co.jp048-720-8352

Outcome results

None listed

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