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A study on the effect of LAB (heat-killed) on Visceral Fat.

A study on the effect of Lactobacillus brevis KB290 (heat-killed) on Visceral Fat. - A study on the effect of Lactobacillus brevis KB290 (heat-killed) on Visceral Fat.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000037620
Enrollment
120
Registered
2019-08-24
Start date
2019-08-24
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

None listed

Interventions

A beverage not containing heat-killed Labre per day for 12 weeks. A beverage containing heat-killed Labre (low-dose) per day for 12 weeks. A beverage containing heat-killed Labre (high-dose) per day f

Sponsors

Kagome Co., Ltd.
Lead Sponsor
KSO Corporation
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Japanese male and female aged 20 to 64 years-old at acquisition of the consent. (2)Whose BMI are 23 or more and less than 30 at screening test. (3)Who can make self-judgment, voluntarily agreed to participate to this study, and provide written informed consent.

Exclusion criteria

Exclusion criteria: (1)Who use medicines that may affect obesity, hyperlipidemia, lipid metabolism. (2)Who has such serious diseases as liver disease, cardiovascular disease, respiratory disease, endocrine disorder, metabolic disease, food allergy disease. (3)Who cannot stop intake health foods or supplements which may affect obesity, hyperlipidemia, lipid metabolism, during this study. (4)Who has a current or history of drug dependence and/or alcoholism. (5)Who has been implanted metal in the DUAL SCAN measurement site. (6)Who has implantable medical devices (e.g., cardiac pacemaker and/or implantable defibrillator). (7)Who has been diagnosed as familial hyperlipidemia. (8)Who is pregnant or breast-feeding or willing to be pregnant during this study. (9)Who has an irregular diet, and/or is shift worker and/or midnight-shift worker. (10)Who is planning to participate and/or has participated in other clinical studies. (11)Who is judged as unsuitable for this study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Visceral fat area

Secondary

MeasureTime frame
Abdominal subcutaneous fat area, total fat area, body weight (BMI), blood pressure, body fat percentage, muscle mass, waist/hip circumference, AST (GOT), ALT (GPT), gamma-GTP, total cholesterol, HDL-cholesterol, LDL-cholesterol, triglycerides, blood glucose level, insulin, HbA1c, HOMA-IR, fecal microbiota.

Countries

Japan

Contacts

Public ContactYoshika Komori

KSO Corporation Sales department

yoshi@kso.co.jp03-3452-7733

Outcome results

None listed

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