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Examination of the effects of PD intake on autonomic nervous function in healthy adults: A Randomized, Double-blind, Placebo-controlled, Crossover Study.

Not Applicable
Conditions
one
Registration Number
JPRN-UMIN000029811
Lead Sponsor
Otsuka Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
48
Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects who have allergic reaction to drug or food. 2) Subjects who have a severe past medical history, acute infection, mental disorder, serious complications or need emergency medical care. 3) Subjects who are under treatment for insomnia, sleep disorder, dysautonomia or endocrine disease. 4) Subjects who expected big change in living environment from 1 month before this study to the end of the study. 5) Subjects who donated either 400 mL whole blood within 12 weeks or 200 mL whole blood within 4 weeks or blood components within 2 weeks prior to this study. 6) Subjects who get an intense exercise. 7) Subjects who are heavy smokers (more than 20 cigarettes per day). 8) Subjects who are alcohol addicts. 9) Subjects who take a drink with high content of caffeine excessively. 10) Subjects who regularly take a drink with high content of theanine. 11) Subjects who have an extremely irregular eating pattern and work the shift or work on midnight. 12) Subjects who are pregnant, lactating or expected to be pregnant during the study. 13) Subjects who regularly take medicine, food for specified health uses, foods with function claims and / or health food which would affect the result of the study. 14) Subjects who are participating in other clinical trials or have participated in other clinical trials within 4 weeks prior to the study. 15) Subjects who have difficulty in compliance with recording of various surveys. 16) Subjects who are judged as unsuitable for the study by the principal investigator for other reasons.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Autonomic nervous function during stress load
Secondary Outcome Measures
NameTimeMethod
Autonomic nervous function and endocrine function during resting state
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