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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02926118
Study type Interventional
Source Unilever R&D
Contact
Status Completed
Phase N/A
Start date April 27, 2017
Completion date October 18, 2017

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