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Clinical Trial Summary

This study aimed at determining the 4-hours postprandial blood glucose and insulin responses to the ingestion of cereal product differing by their SDS content.


Clinical Trial Description

This study aimed at determining the 4-hours postprandial blood glucose and insulin responses to the ingestion of cereal product differing by their SDS content. It is a laboratory-based research study with an open cross-over design, including 20 healthy non-smoking voluntary subjects, aged from 18 to 45 years. 2 test sessions per subject are included in the study. Foods are consumed in a random order according to a randomisation list. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02538653
Study type Interventional
Source Mondelez International, Inc.
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date December 2015