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Clinical Trial Summary

The purpose of this study is to compare the effects of PROMITOR® Soluble Corn Fiber versus inulin on GI symptoms (tolerance), stool consistency (laxation) and fecal microbiome at levels that could contribute to closing the fiber gap. The dose response effects of PROMITOR® Soluble Corn Fiber in healthy children will also be compared.


Clinical Trial Description

After initial site visits and randomization children were given a packet of powdered fiber to be mixed into a beverage daily. There were four test arms, described elsewhere. Each study arm lasted 10 days with an 18 day washout in between study periods. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05213494
Study type Interventional
Source Tate & Lyle
Contact
Status Completed
Phase N/A
Start date May 20, 2021
Completion date October 28, 2021

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