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A confirmation study of the effect on human basal metabolism by consumption of the food which contains plant extract

A confirmation study of the effect on human basal metabolism by consumption of the food which contains plant extract - An effect study of plant extract on human basal metabolism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028982
Enrollment
40
Registered
2017-09-06
Start date
2017-09-07
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 male adult

Interventions

Test food consumption, 5 weeks for efficiency evaluation, within 7 weeks for safety evaluation.-Washout 5 to 12 weeks-Control food consumption, 5 weeks for efficiency evaluation, within 7 weeks for sa

Sponsors

CPCC Company Limited
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Healthy males aged 20 to 49 years old. 2)Subjects whose body mass index (BMI) is 19.0 kg/m2 to 29.9kg/m2 3)Subjects whose visceral fat area is less than 100cm2 4)Subjects who have constant life cycle and custom to go to bed until around 1 a.m. 5)Subjects giving written informed consent.

Exclusion criteria

Exclusion criteria: 1)Subjects who have severe disease in liver, kidney, heart, lung, digestive organ, blood, endocrine system and metabolic system. 2)Subjects who are receiving treatment or medication at the giving point of informed consent. 3)Subjects who have a history of allergic reaction or hypersensitivity to drug medicine and food. 4)Subjects who have a smoking habit. 5)Subjects who drink alcohol a lot. 6)Subjects who have midnight work or irregular shift work. 7)Subjects who cannot stay and lodging in the facility four times. 8)Subjects who are concerned about rashes and itching by attaching electrode pad. 9)Subjects who have no response in power spectrum of heart rate variability after stimulation of autonomic nerve system. 10)Subjects who are participating in the other clinical tests. Subjects who participated within 1 month prior to the current study and/or who plan to participate in the other clinical tests. 11)Subjects who have been judged as unsuitable for the study by the principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Basal metabolic rate

Secondary

MeasureTime frame
*Heart rate *Deep body temperature *Sleep situation

Countries

Japan

Contacts

Public ContactMakoto Ichinohe

CPCC Company Limited Plan Sales Department

cpcc-contact@cpcc.co.jp03-5297-3112

Outcome results

None listed

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