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A study for evaluating the effect of the intake of the test products on postprandial hyperglycemia for healthy male

A study for evaluating the effect of the intake of the test products on postprandial hyperglycemia for healthy male - A study for evaluating the effect of the intake of the test products on postprandial hyperglycemia for healthy male

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025996
Enrollment
12
Registered
2017-02-03
Start date
2017-02-04
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 male

Interventions

Intake of the standard products,Intake of the test products

Sponsors

TTC Co.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1)Males from 20 to 50 years of age. (2)Subjects who have a difference of incremental area under the curve of plasma glucose levels between preliminary examination 1 and preliminary examination 2 within 25 percent.

Exclusion criteria

Exclusion criteria: (1)Subjects routinely taking medicine or health food which may influence glucose metabolism. (2)Subjects who have abnormal glucose tolerance within the one month prior on preliminary examination. (3)Subjects who have body mass index (BMI) less than 18.5 kg per square meter or more than 25.0 kg per square meter. (4)Subjects who have abnormal glucose tolerance on preliminary examination (5)Subjects who work at night or have irregular life more than one time in the study. (6)Subjects who are planning to go overseas. (7)Subjects with allergies to the test food in the study. (8)Subjects who drink alcohol a lot. (9)Subjects who smoke a lot. (10)Subjects who has serious illness such as diabetes, liver disease, kidney disease, heart disease, digestive system disease. (11)Subjects who have a disease under medication or having a history of study such as obesity, dyslipidemia, hypertension or who has a serious disease. (12)Subject who are judged as unsuitable for the study from clinical measurements for preliminary tests and measurements. (13)Subjects who have participated in other clinical study within the last one month or have planned to participate other clinical studies. (14)Subjects who are judged as unsuitable for the study from questionnaire. (15)Subjects who are judged as ineligible by clinical investigator.

Design outcomes

Primary

MeasureTime frame
Incremental area under the curve of plasma glucose

Secondary

MeasureTime frame
Peak in plasma glucose concentration, fasting plasma glucose , plasma glucose at 15, 30, 45, 60, 90, and 120 min.

Countries

Japan

Contacts

Public ContactNoriko Watanabe

TTC Co.,Ltd. Clinical Research Planning Department

n.watanabe@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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