A clinical study to evaluate the effects of dextrin on maintaining hydration status
- 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
Not provided
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
Name Time Method
- Secondary Outcome Measures
Name Time Method