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Effect of a plant-derived ingredient containing food on lipid metabolism.

Effect of a plant-derived ingredient containing food on lipid metabolism. - Efflcacy of a plant-derived ingredient containing food for postprandial lipid metabolism.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020151
Enrollment
30
Registered
2015-12-18
Start date
2015-12-21
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 adults

Interventions

Single ingestion of plant-derived ingredient containing food (test food code: A001)-&gt
Single ingestion of plant-derived ingredient not containing food (control food code: P001). Single ingestion of plant-derived ingredient not containing food (control food code: P001))-&gt
Single ingestion of plant-derived ingredient containing food (test food code: A001).

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy males and females.

Exclusion criteria

Exclusion criteria: 1. difficult to participate the study due to dysfunctions liver, or the other dysfunctions. 2. experienced a seizures based on circulatory-diseases before, or is under treatment. 3. arrhythmic. 4. who takes medication for glucose or fat metabolism, or hypertention. 5. who have experienced a seizures based on neural disease. 6. who was given surgery for a disease or an injury 2 months prior to the study. 7. who was given gastrectomy and/or bypass of part of the intestine. 8. who have allergic reaction for food. 9. Individual experienced unpleasant feeling during blood drawing. 10. claustrophobia. 11. insomnia. 12. chronic headache (migraine, tension headache, cluster headache, etc. ). 13. Person who donated more than 200mL of blood within a month, or more than 400mL within three months prior to informed consent. 14. who sleep habitually after 1:00 a.m. on weekday. 15. Heavy smoker 16. who had a weight change of more than +-2.0 kg for one month prior to informed consent. 17. who is engaged in night work and shift operations for more than 3 months prior to informed consent. 18. who is pregnant or expecting pregnancy. 19. who habitually take the foods for specified health uses (FOSHU) or functional food which solicits body fat reduction and absorption suppression of lipid or the carbohydrates (except for person who can stop consume them after informed consent.). 20. who can't accept doctor to check health condition, accessing the health examination result for the past two years, prior to the study. 21. who can't disclose age, the latest health examination result. 22. who can't reply to the questionnaire about living situation and condition. 23. who cannot indicate a menstruation situation.

Design outcomes

Primary

MeasureTime frame
8 hours of postprandial fat oxidation measurement by human calorimeter.

Secondary

MeasureTime frame
8 hours of postprandial energy expenditure and respiratory quotient measurement by human calorimeter.

Countries

Japan

Contacts

Public ContactToshitaka Sakuda

Kao Corporation R&D-Development Research-Healthcare Food Research

sakuda.toshitaka@kao.co.jp03-5630-7456

Outcome results

None listed

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