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A clinical study to evaluate the effects of dextrin on maintaining hydration status

Not Applicable
Conditions
one
Registration Number
JPRN-UMIN000031443
Lead Sponsor
Soiken Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
12
Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects having serious hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders 2) Subjects who have a seasonal allergic rhinitis (cedar or Japanese cypress pollen) with moderate or severe symptoms 3) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 4) Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 5) Subjects deemed unsuitable by the investigator

Study & Design

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