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A randomized controlled trial for effect of alcohol metabolism.

A randomized controlled trial for effect of alcohol metabolism. - A randomized controlled trial for effect of alcohol metabolism.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014995
Enrollment
15
Registered
2014-08-29
Start date
2014-02-13
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 volunteer

Interventions

Sequence:Turmeric containing supplements -wash out-placebo Sequence:placebo-wash out-Turmeric containing supplements

Sponsors

CPCC Company Limited
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Subjects who is male and 20 years of age or older at the time of informed consent. 2)Subjects who is drinking possible. 3)Subjects who can make self-judgment and are voluntarily giving written informed consent.

Exclusion criteria

Exclusion criteria: 1)Subjects who have previous medical history of drug and/or food allergy. 2)Subjects who have previous medical history and/or current medical history of serious diseases (e.g., diabetes, digestive organ, liver, pancreas, heart and/or kidney). 3)Subjects who have been enrolled in the other clinical trials within about last 1 month. 4)Subjects who predicted gluttony and irregular eating habits by the pre-questionnaire and doctor's questions. 5)Subjects who constantly use supplements and/or functional foods affecting alcohol metabolism.(e.g. Turmeric-containing foods and beverages) 6)Subjects who can't drink alcohol. 7)Subjects who excessive alcohol intake. 8)Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study. 9)Subjects who have donated over 400 mL of blood and/or blood components within the last three months prior to the current study. 10)Subjects who collected blood amount of blood sampling over 1200 mL within the last twelve months prior to the current study and this clinical trial's blood sampling. 11)Subjects who take medicines and plan to take new health foods. 12)Others who have been determined ineligible by principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Blood alcohol concentration Blood acetaldehyde concentration

Secondary

MeasureTime frame
Physical examinations Blood test Urine test Breath alcohol concentration Questionnaires(bodily sensation)

Countries

Japan

Contacts

Public ContactMakoto ICHINOHE

CPCC Company Limited Plan sales department

cpcc-contact@cpcc.co.jp03-5927-3112

Outcome results

None listed

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