Bioavailability and Dosing of a Monosaccharide Supplement in Adults
NCT ID: NCT00782392
Last Updated: 2011-05-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
15 participants
OBSERVATIONAL
2007-01-31
Brief Summary
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Many of these sugars have been used in a glyco-nutritional supplement in adults and children, with minimal or no reported side effects.
We are developing a custom blend of important individual sugars, and need information regarding their dosing and blood concentrations following oral intake of the carbohydrate supplement. Timed blood samples following the carbohydrate supplement will provide us with a better understanding of the most effective dose and the metabolism of these sugars in adults. This will give us the preliminary information we need for developing an oral supplement of special sugars that can be added to infant formulas to help improve brain development and immune function in infants and children.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* Male
* Age 18-28
* Regularly eat breakfast
* Healthy
* BMI within normal limits (18.5 - 24.9)
* English speaking
Exclusion Criteria
* Chronic medical diagnosis
* Medications that may interfere with the study
18 Years
28 Years
MALE
Yes
Sponsors
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University of Arkansas
OTHER
United States Department of Agriculture (USDA)
FED
Arkansas Children's Hospital Research Institute
OTHER
Responsible Party
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University of Arkansas for Medical Sciences
Locations
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Arkansas Children's Nutrition Center
Little Rock, Arkansas, United States
Countries
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Other Identifiers
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45092
Identifier Type: -
Identifier Source: org_study_id
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