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An evaluation study for fat metabolism improving effect by single consumption of test beverage

An evaluation study for fat metabolism improving effect by single consumption of test beverage - An evaluation study for fat metabolism improving effect by single consumption of test beverage

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039405
Enrollment
40
Registered
2021-02-06
Start date
2020-02-07
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 adults

Interventions

Intake of test beverage just before measuring metabolism by exhalation - Measuring metabolism by exhalation. Rest period (over 5 days). Intake of control beverage just before measuring metabolism by

Sponsors

CPCC Company Limited
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Healthy males aged 20 to under 40 years old. 2) Males whose have no custom of exercise. 3) Males whose BMI ranges from 18.5 to 25.0 4) Males who receive enough explain of the test, who deeply understanding of the test, and who obtain own consent to participate the test.

Exclusion criteria

Exclusion criteria: 1) Males who have previous and/or current medical history of serious disease (e.g., circulatory organs, respiratory organs, digestive organs, urinary organs and endocrine organs). 2) Males who constantly use or who can't restrict use oral medicines (related to blood pressure, fatigue and fat metabolism) having a possibility of affecting test results. 3) Males who constantly use or who can't restrict use supplements, vitamins and nutrient (related to blood pressure, blood flow, exercise fatigue, metabolic improvement, fat burning or lipolysis) having a possibility of affecting test results. 4) Males who excessive alcohol intake. 5) Male who may interfere with the operation of the test due to allergic rhinitis. 6) Males who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study. 7) Males who have smoking habit. 8) Males who are severe anemia 9) Males who have previous medical history of drug and/or food allergy. 10) Males who donated over 200mL blood and/or blood components within the last one month to this study. 11) Males who donated over 400mL blood and/or blood components within the last three months to this study. 12) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 13) Others who have been determined ineligible by principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Respiration quotient

Secondary

MeasureTime frame
Fat oxidation Energy expenditure Skin surface temperature of back Incidence of adverse events and of side effects

Countries

Japan

Contacts

Public ContactMakoto Ichinohe

CPCC Company Limited Planning & Sales Department

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

Outcome results

None listed

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