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CompletedNCT00782392Updated May 18, 2011

Bioavailability and Dosing of a Monosaccharide Supplement in Adults

An observational study in Healthy Males, sponsored by Arkansas Children's Hospital Research Institute. Completed at 1 site in United States. Open to male participants aged 18 Years to 28 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-05-18.

Sponsored by Arkansas Children's Hospital Research Institute · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
15
Ages
18 Years to 28 Years
Sex
Male
01

Study summary

We are developing an oral supplement of carbohydrates to be added to infant formulas in order to improve brain development, immune function, and overall health of infants and children. After a careful review of what is known about these sugars, there is very little information regarding their use in infants and children, although there is some information in adults and animals.

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.

02

Conditions studied

  • Healthy Males

Keywords

  • Nutrition
  • Infant Formula
03

In context

Lead sponsor

Arkansas Children's Hospital Research Institute is the lead sponsor of 118 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 28 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Healthy Caucasian Males

Inclusion criteria

  • Caucasian (non-hispanic)
  • Male
  • Age 18-28
  • Regularly eat breakfast
  • Healthy
  • BMI within normal limits (18.5 - 24.9)
  • English speaking

Exclusion criteria

Exclusion Criteria:

  • History of smoking, more than occasional alcohol use, or drug use.
  • Chronic medical diagnosis
  • Medications that may interfere with the study
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
15 participants (actual)
Biospecimen retention
Samples without dna
06

Study locations

1 site
  • Arkansas Children's Nutrition Center
    Little Rock, Arkansas 72202, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 18, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00782392
Lead sponsor
Arkansas Children's Hospital Research Institute
Collaborators
University of Arkansas, United States Department of Agriculture (USDA)
First posted
Oct 31, 2008
Start date
Jan 2007
Primary completion
Jun 2007
Last update
May 18, 2011

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2011. You cannot join it, but the record below documents what was studied.

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