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Effect of fragmented Lactobacillus amylovotus CP1563 on substrate oxidation and energy expenditure: a randomized cross-over trial

Effect of fragmented Lactobacillus amylovotus CP1563 on substrate oxidation and energy expenditure: a randomized cross-over trial - Effect of fragmented Lactobacillus amylovotus CP1563 on energy metabolism

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023927
Enrollment
15
Registered
2016-09-04
Start date
2016-08-01
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

Ingestion of Lactobacillus amylovorus CP1563for 3 weeks, Wash out 1 week and ingestion of Placebo for 3 weeks. Ingestion of placebo for 3 weeks, Wash out 1 week and ingestion of Lactobacillus amylovor

Sponsors

Fukuoka university
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) Subjects who can make self-judgment and are voluntarily giving written informed consent. 2) Males whose age 40 to 59 years old for Japanese.

Exclusion criteria

Exclusion criteria: 1. Subjects who have diabetes in the second degree. 2. Subjects who have past surgical historyof gastroenterological surgery. 3. Subjects who use pharmaceuticals regularly. 4. Subjects who have an acute disease like a inflammation of the upper airway or acute gastroenteritis. 5. Subjects who excessive alcohol intake and who have a smoking habit. 6. Subjects with allergies of lactobacillus, milk, soy and citrus. 7. Subjects who is irregular eating habits. 8. Subjects who are participating or will participate other clinical trials. 9. Others who have been determined ineligible by principal investigator or subinvestigator.

Design outcomes

Primary

MeasureTime frame
Energy expenditure, Fat oxidation

Countries

Japan

Contacts

Public ContactYoichi Hatamoto

Fukuoka univercity Faculty of Sports and Health Science

y.hatamoto.7@gmail.com+81-92-871-6631

Outcome results

None listed

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