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Study on post-drinking performance after ingestion of test foods

Study on post-drinking performance after ingestion of test foods - Study on post-drinking performance after ingestion of test foods

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052168
Enrollment
5
Registered
2023-09-11
Start date
2023-09-11
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

Total of 600 mg of the test food before and after drinking alcohol (180 mL of clear alcohol (15% alcohol)). Washout for 1week or more. Total of 600 mg of the placebo before and after drinking alcoho

Sponsors

Healthcare Systems Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document 2.Japanese who are 20 years old or more and under 64 years old 3.Persons who are aware of a decline in performance the day after drinking

Exclusion criteria

Exclusion criteria: 1.Persons who have chronic illness, receiving medication, have a serious disease history 2.Persons who are allergic to the test food or alcohol 3.Persons who normally consume large amounts of the test food 4.Persons who regularly use medicines or foods with health claims (foods for specified health use, foods with functional claims and foods with nutritional claims) etc., that may affect alcohol metabolism and sleep quality 5.Persons who have participated in other tests within the past one month before the start of test, or those who intend to participate in another exam after consenting to the exam 6.Persons who were judged as inappropriate for study participant by the principal investigator 7.Persons who are breast-feeding, pregnant and planning or wishing to become pregnant during the study period

Design outcomes

Primary

MeasureTime frame
Uchida Kraepelin test

Secondary

MeasureTime frame
VAS questionnaire on physical condition OSA sleep inventory MA version Brain waves ADH1C and ADH1B polymorphisms

Countries

Japan

Contacts

Public ContactKosei Nishikawa

Healthcare Systems Co., Ltd. Clinical Research Department

nishikawa@hc-sys.jp03-6809-2722

Outcome results

None listed

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