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Clinical Trials/JPRN-UMIN000037071
JPRN-UMIN000037071
Completed
未知

A study for measurement of Glycemic Index (GI) of two kinds of foods in adult males and females - A study for measurement of Glycemic Index (GI) of two kinds of foods

TTC Co., Ltd.0 sites12 target enrollmentJune 14, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
TTC Co., Ltd.
Enrollment
12
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 14, 2019
End Date
September 30, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
TTC Co., Ltd.

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Subjects routinely taking medicine or health food which may influence glucose metabolism (2\) Subjects whose BMI exceeds 30\.0 kg/m2 (3\) Subjects whose blood glucose level exceeds 126 mg/dL (4\) Subjects who have been pointed out as impaired glucose tolerance within 1 year (5\) Subjects who are suspected as impaired glucose tolerance in preliminary examination (6\) Subjects whose blood glucose level exceeds 110 mg/dL in glucometer on admission (7\) Subjects planned to travel abroad during the study period (8\) Subjects having possibilities for emerging allergy related to the current study (9\) Subjects who drink much alcohol (10\) Subjects who do excessive smoking (11\) Subjects who donated blood (blood donation etc.) exceeding 200 mL within 1 month or 400 mL within 4 months (12\) Subjects who have under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (13\) Subjects who have under treatment (e.g.,adiposity,hyperlipidemia, hypertension) that affects the evaluation of this study or medical history of serious illness for medication (14\) Subjects whose values of physical measurement, physical examination and clinical laboratory are significantly different from the reference range (15\) Subjects who may be pregnant or are pregnant, breastfeeding, or those who desire pregnancy during the study period (16\) Subjects who have participated in other clinical study within the last one month or have plan to participate other clinical studies (17\) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (18\) Subjects who are judged as ineligible by the clinical investigator

Outcomes

Primary Outcomes

Not specified

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