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A study to investigate Postprandial blood glucose level increase suppressing effect of study food ingestion

A study to investigate Postprandial blood glucose level increase suppressing effect of study food ingestion - A study to investigate Postprandial blood glucose level increase suppressing effect of study food ingestion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000033442
Enrollment
20
Registered
2018-07-20
Start date
2018-08-08
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

None

Interventions

Sponsors

CROee.INC
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Subjects who is healthy adults of both sexes above 20 years old- under 65 years old 2)Subjects with fasting blood glucose level under 125mg/dL, and under 199mg/dL after food load at the point of screening 3)Subjects who give consent in writing with full understanding

Exclusion criteria

Exclusion criteria: 1)Subjects who has difficulties to participate this study due to hepatic, kidney, cardiac disorders, lung disorder, digestive system disorder, blood disorder, endocrine disorder, metabolic defect and other serious disorders. 2)Subjects who suffer from diseases/ disorders with continuous medical treatment or with medical history of severe diseases/ disorders needed medical treatment 3)Subjects who suffer from diseases/ disorders that affects the study and are receiving medical treatment from medical institution or have surgical history of digestive system ( except appendectomy) 4)Subjects with history of sensitivity to the ingredients of test food 5)Pregnant, lactating women or willing to be pregnancy during the study 6)Subjects who had participated in other clinical trials including drug and food within 1 month. 7)Any candidates considered to be unsuitable for enrollment in the opinion of the principal investigator

Design outcomes

Primary

MeasureTime frame
Postprandial blood glucose level (AUC,C-Max)

Secondary

MeasureTime frame
Awareness questionnaire

Countries

Japan

Contacts

Public ContactShigeru Imai

CROee.INC Evidence Division

imai@croee.com03-5953-2108

Outcome results

None listed

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