Trials / Completed
CompletedNCT02926118
Continuous Glucose Monitoring During Diets That Differ in Glycemic Load
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 23 (actual)
- Sponsor
- Unilever R&D · Industry
- Sex
- All
- Age
- 50 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
This study test whether a Continuous Glucose Monitor can pickup differences in glucose (in the interstitial fluid) during a dietary intervention using meals with either a high with a low glycemic load.
Detailed description
The aim of this study is to determine the suitability of a continuous glucose monitor to detect the impact of a dietary intervention on postprandial blood glucose levels in normal, healthy, free living subjects. We will compare a dietary intervention of meals with a high glycemic load (high post-meal blood glucose) versus meals with a low glycemic load (low post-meal blood glucose) in a cross-over study. In addition, the glucose profiles obtained both via venous blood sampling and via continuous glucose monitor following a standard carbohydrate load will be compared.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Low glycemic load | Low glycemic load diets will be consumed at breakfast, lunch and dinner for three consecutive days |
| DIETARY_SUPPLEMENT | High glycemic load | High glycemic load diets will be consumed at breakfast, lunch and dinner for three consecutive days |
Timeline
- Start date
- 2017-04-27
- Primary completion
- 2017-07-13
- Completion
- 2017-10-18
- First posted
- 2016-10-06
- Last updated
- 2017-10-19
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT02926118. Inclusion in this directory is not an endorsement.