Clinical Trials Directory

Trials / Completed

CompletedNCT02538640

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

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

Summary

This is a laboratory-based research study conducted in two parts. Open cross-over design. 2 test sessions per subject included in the study. It aims at determining the postprandial blood glucose and insulin responses to the ingestion of cereal product differing by their SDS content and GI in 20 healthy non-smoking voluntary subjects, aged from 18 to 45 years.

Detailed description

This is a laboratory-based research study conducted in two parts. Open cross-over design. 2 test sessions per subject included in the study. It aims at determining the postprandial blood glucose and insulin responses to the ingestion of cereal product differing by their SDS content and GI in 20 healthy non-smoking voluntary subjects, aged from 18 to 45 years.

Conditions

Interventions

TypeNameDescription
OTHERHigh-SDS biscuitConsumption of the high-SDS product (50g) alone with a glass of water
OTHERLow-SDS extruded cerealsConsumption of the low-SDS product (42g) alone with a glass of water

Timeline

Start date
2015-08-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2015-09-02
Last updated
2015-11-02

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT02538640. Inclusion in this directory is not an endorsement.