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A study for evaluating the effects of oral intake of alcohol beverages on biological responses. A double-blind, three-way cross-over trial

A study for evaluating the effects of oral intake of alcohol beverages on biological responses. A double-blind, three-way cross-over trial - A study for evaluating the effects of oral intake of alcohol beverages on biological responses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020649
Enrollment
36
Registered
2016-01-25
Start date
2016-01-28
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 (Healthy adults)

Interventions

One sample is taken and biological responses are measured every day for 3 straight days. 5% alcohol (day 1), 3% alcohol (day 2), 0% alcohol (day 3) in order. One sample is taken and biological respons

Sponsors

CPCC Company, Limited
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Males aged from 20 to less than 30 years old and weighted from 58 kilograms to less than 72 kilograms, when giving the informed consent. 2)Individuals who can drink and does not dislike chuhai. 3)Individuals who show NN (normal/normal) or ND (normal/deficient) in the alcohol patchtest 4)Individuals whose biological responses can be suitably measured. 5)Individuals who give the informed consents in writing, after receiving enough explanation of the purpose and details of the study, understanding the study well, and deciding to attend the study with their own will.

Exclusion criteria

Exclusion criteria: 1)Individuals who cannot drink alcohol beverages and / or have alcohol allergy. 2)Individuals who cannot stop drinking alcohol beverages the day before the checkup except for the test beverages during this study. 3)Individuals who use medicines which have possible effects on mental condition continuously. 4)Individuals who have under treatment or a history of drug addiction and / or alcoholism. 5)Individuals who have a history of mental diseases and / or epilepsy. 6)Individuals who have a plan to drive a car and operate a machine. 7)Individuals who have drug and / or food allergy. 8)Individuals who are participating in other clinical trials of drugs or health food, who participated in the last 4 weeks, or who are willing to participate after giving the informed consent. 9)Individuals who have a smoking habit. 10)Individuals who are judged unsuitable for this study by the investigators for other reasons.

Design outcomes

Primary

MeasureTime frame
Evaluation of physiological measures including breath ethanol, indexes of autonomic and central nervous systems for one hour after intervenstion

Secondary

MeasureTime frame
Evaluation of emotions using questionnaire survey for one hour after intervenstion

Countries

Japan

Contacts

Public ContactMasanori Numa

CPCC Company, Limited Sales department

m.n@cpcc.co.jp03-5297-3112

Outcome results

None listed

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