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Clinical Trial Summary

Participants will be randomly assigned to either regular or no-carrageenan prepared diets to determine whether the no-carrageenan leads to improvement in glucose tolerance. Hemoglobin A1c is the primary outcome measure.


Clinical Trial Description

Subjects will be randomly assigned to a diet. They will at onset have hemoglobin A1c values between 5.7% and 6.4%. Baseline glucose tolerance test will be performed, as well as measures of inflammation and fecal microbiome. Interim tests will be performed at six weeks. Subjects will participate for 12 weeks, at which time they will be re-evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02720393
Study type Interventional
Source University of Illinois at Chicago
Contact
Status Completed
Phase N/A
Start date February 2016
Completion date December 2018

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