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A study for the effect on appetite by food intake

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000037914
Lead Sponsor
TTC Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who continuously take health foods related to rich in lactic acid bacteria for over once a week (2) Subjects who continuously take medicine and health foods related to glycometabolism and appetite more than once a week (3) Subjects who have the exercise habits more than twice a week (4) Subjects who have meat skipping once and more a week (5) Subjects with alcohol drinking habit more than three times a week (6) Subjects who have the habit of taking foods high in lactic acid bacteria (fermented milk drink, yoghurt, kimuchi, and so on) and/or lactic acid bacteria preparations twice and more a week (7) Subjects who are judged as bulimia in BITE (8) Subjects who have or has medical history serious illness such as diabetes, liver disease, kidney disease, heart disease (9) Subjects who has chronic illness or have medical history of serious illness for medication (10) Subjects who have possibilities for emerging allergy onset related to the study (11) Subjects who was given or donated 200 ml or 400 ml whole blood within three months before pre-inspection (12) Subjects who are judged as unsuitable for the study because of clinical test, anthropometric test and physical examination in pre-inspection (13) Subjects who have participated in other clinical study within the last one month or have plan to participate other clinical studies (14) Subjects who are pregnant or lactating, or plan to become pregnant or lactate during the study (15) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (16) Subjects who are judged as unsuitable for the study by investigator for other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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