Clinical Trials Directory

Trials / Completed

CompletedNCT02538653

Determination of the Postprandial Responses to Two Cereal Foods Differing by Their SDS Content Consumed Alone.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Mondelēz International, Inc. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERSandwich biscuit high in SDSConsumption of the high SDS product (50g) alone with a glass of water
OTHERCo-extruded cereal low in SDSConsumption of the low SDS product (48.3 g) alone with a glass of water

Timeline

Start date
2015-09-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2015-09-02
Last updated
2017-09-14

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT02538653. Inclusion in this directory is not an endorsement.