Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTLow glycemic loadLow glycemic load diets will be consumed at breakfast, lunch and dinner for three consecutive days
DIETARY_SUPPLEMENTHigh glycemic loadHigh 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.