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A study for the effect on appetite by food intake

A study for the effect on appetite by food intake - A study for the effect on appetite by food intake

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000037914
Enrollment
80
Registered
2020-11-30
Start date
2019-09-04
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 adult

Interventions

Ingestion of food containing Lactic acid bacteria for 4 consecutive weeks Ingestion of placebo without Lactic acid bacteria for 4 consecutive weeks

Sponsors

TTC Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Male and female aged from 20 to 69 (2) Subjects who are aware of overeating tendencies, but who were judged healthy by the investigator (3) Subjects with BMI greater than 25.0 and less than 30.0 kg / m2

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Questionnaire on feeling of fullness and apptite(SNAQ-JE,Visual analogue scale)at 4 week ingestion

Secondary

MeasureTime frame
GLP-1 value,Bulimic Investigatory Test Edinburgh and dietary intake at 4 week

Countries

Japan

Contacts

Public ContactKunihiko Wasaki

TTC Co., Ltd. Clinical Research Planning Department

k.wasaki@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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