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Effect of Daily Ingestion of the potatoes on improving minor ailments: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study

Not Applicable
Conditions
Healthy adults
Registration Number
JPRN-UMIN000038876
Lead Sponsor
Hokkaido Information University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
16
Inclusion Criteria

Not provided

Exclusion Criteria

1.Subjects who are under physician's advice, treatment, and/or medication for schizophrenia, depression, mania, neurological disorders, and/or sleep disorders. 2.Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 3.Subjects with major surgical history relevant to the digestive system such as gastrectomy, gastrorrhaphy, enterectomy, etc. 4.Subjects with unusually high and/or low blood pressure and/or abnormal hematological data. 5.Subjects with severe anemia. 6.Pre- or post-menopausal women complaining of obvious physical changes. 7.Subjects who are at risk of having allergic reactions to drugs or foods especially based on potatoes, Betulaceae, Poaceae. 8.Subjects who regularly take medicine, functional foods, and/or supplements which would affect sleep and/or stress. 9.Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 10.Subjects who donated either 400 ml whole blood within 16 weeks (women), 12 weeks (men), 200 ml whole blood within 4 weeks (men and women), or blood components within 2 weeks (men and women), prior to the current study. 11.Pregnant or lactating women or women who expect to be pregnant during this study. 12.Subjects who currently participate in other clinical trials, or participated within the last 4 weeks prior to the current study. 13.Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.

Study & Design

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