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A study for the effect of intake of lactic acid bacteria on abdominal fat

A study for the effect of intake of lactic acid bacteria on abdominal fat - A study for the effect of intake of lactic acid bacteria on abdominal fat

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051324
Enrollment
80
Registered
2024-12-01
Start date
2023-06-14
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

Sponsors

EP Mediate Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy males and females from 20 to 64 years of age 2. Subjects whose BMI is 23kg/m2 or more and less than 30kg/m2 3. The average blood pressure, triglycerides, HDL-cholesterol, and blood glucose of the people starting intake should be within the reference range for each item

Exclusion criteria

Exclusion criteria: 1. Subjects who regularly ingest food, health food or medicine rich in lactic acid bacteria or natto bacteria 2. Subjects who regularly ingest health food or medicine that affects body fat and lipid metabolism 3. Subjects who are judged to be unsuitable for research from the results of the screening test 4. Subjects who may develop allergies related to the study 5. Subjects who exercise excessively 6. Subjects who are on a diet at the time of the screening test 7. Subjects who have a disease requiring regular administration, or who have a history of severe disease 8. Subjects whose physical measurement values, blood pressure values, and clinical inspection values are significantly outside the reference range before starting intake 9. Subjects who have or have a history of a severe disease 10. Subjects who drink a lot 11. Subjects who are judged to be unsuitable for the study based on the results of lifestyle questionnaires 12. Subjects who donated blood within one month before the study 13. Subjects who have participated in other clinical study within one month before the study or plan to participate in other clinical study after informed consent to the study 14. Subjects who are pregnant or breastfeeding, or plan to do so during this study 15. Subjects judged as unsuitable for the study by a doctor

Design outcomes

Primary

MeasureTime frame
Abdominal fat

Secondary

MeasureTime frame
waist circumference, hip circumference, waist circumference / hip circumference, body weight, BMI, body fat percentage, blood index

Countries

Japan

Contacts

Public ContactTakashi Nakagawa

EP Mediate Co., Ltd. Foods Department, Trial Planning Section 2

nakagawa.takashi768@eps.co.jp080-7710-1146

Outcome results

None listed

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