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
| Type | Name | Description |
|---|---|---|
| OTHER | High-SDS biscuit | Consumption of the high-SDS product (50g) alone with a glass of water |
| OTHER | Low-SDS extruded cereals | Consumption 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.