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Study on effects of a plant-derived protein containing food product on postprandial hyperglycemia

Not Applicable
Conditions
Postprandial hyperglycemia
Registration Number
JPRN-UMIN000014533
Lead Sponsor
Kao Corporation
Brief Summary

There was a significantly difference in the primary outcome between the groups

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1, Person who is difficult to participate the study due to dysfunctions of liver, kidney, heart, respiration, endocrine secretion, metabolism, nervous system, consciousness or diabetes, or the other dysfunctions 2, Person who was given surgery for a disease or an injury 2 months prior to the study 3, Person who was given gastrectomy and/or bypass of part of the intestine 4, Person who takes medication for glucose or fat metabolism, or hypertension 5, Person who habitually consumes the foods for specific health use (FOSHU) and/or dietary supplements (capsules) (except for person who can stop to consume them right after informed consent) 6, Person who is or had been given treatment for allergies to test food ingredients 7, Person who has been ill due to blood collecting 8, Person who donated 200mL or more of blood within a month prior to the study 9, Person who skip breakfast habitually 10, Heavy smoker or person who cannot stop

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
postprandial blood glucose
Secondary Outcome Measures
NameTimeMethod
Insulin, TG, GIP, GLP-1, ghrelin, appetite (satiety)
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