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Physiological effects test by continuous intake of alcohol

Not Applicable
Conditions
Healthy subjects
Registration Number
JPRN-UMIN000044998
Lead Sponsor
HUMA R&D CORP
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
42
Inclusion Criteria

Not provided

Exclusion Criteria

1.Habitual drinkers (subject who drinks more than once a week on average in the last 3 months). 2.Subject who plans to have a health checkup and a human dock test during the test period. 3.Subject who is taking medication or under medical treatment due to serious illness. 4.Subject who is under exercise therapy or dietetic therapy. 5.Subject who may develop allergies (alcohol) due to the test foods. 6.Subject with current or history of alcohol and drug dependence. 7.Subject who is out of the hospital due to mental disorders (depression, etc.) or sleep disorders, or who has a history of mental illness in the past. 8.Subject with irregular life rhythms due to night shifts or shift work. 9.Subject with extremely irregular lifestyle habits such as eating and sleeping. 10.Subject who has an extremely unbalanced diet. 11.Subject who uses health foods, supplements, and medicines that affect alcohol metabolism. 12.Subject who has participated in other clinical studies within the past 3 months from the day of the consent acquisition or who is planning to participate in other clinical studies during the current study. 13.Subject who has blood collection or donation more than 200mL within the past 1 month or more than 400mL within the past 3 months from the day of the consent acquisition. 14.Subject who is planning to get pregnant after the day of informed consent or is currently pregnant and lactating. 15.Subject who has difficulty observing records on various survey forms. 16.Subject who is judged as an inappropriate candidate according to the screening data. 17.Subject who is considered as an inappropriate candidate by the doctor in charge.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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