Clinical Trials Directory

Trials / Completed

CompletedNCT05185960

Comparison of the Postprandial Glycemic and Insulinemic Response of ALLSWEET When Taken Alone or When Added to Sucrose

Comparison of the Postprandial Glycemic and Insulinemic Response of ALLSWEET When Taken Alone or When Added to Sucrose: A Randomized, Double Blind, Controlled Clinical Trial in Healthy Individuals

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Anderson Advanced Ingredients · Industry
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Accepted

Summary

This study will explore the postprandial glycemic response of ALLSWEET®, a non-GMO certified allulose, when consumed alone or with sucrose, compared to the consuming sucrose alone. On 3 separate days, subjects will consume in random order ALLSWEET® alone, ALLSWEET® added to sucrose, or sucrose alone. Blood samples for glucose and insulin analysis with be taken for 2 hours following consumption of the beverages.

Detailed description

Each subject will receive 3 test meals in a double blinded, randomized, crossover fashion. 1. Test arm 1: 30g sucrose 2. Test arm 2: 30g sucrose + 15g of ALLSWEET® 3. Test arm 3: 15g ALLSWEET® All sweeteners will be mixed with 250ml of water. Eligible subjects will be studied on 3 separate days over a period of 4 weeks or less, with at least 1 day in between test days. A fasting fingerprick blood sample will be collected for glucose and insulin analysis after which the test meal will be administered. Additional fingerprick blood samples will be drawn over the next 2 hours (15', 30', 45', 60', 90' and 120' after the first sip of the test drink). Power calculation: A sample size of 15 subjects, is sufficient to detect a 25% difference in incremental area under the curve between meals with 80% statistical power. Statistical Analysis: Incremental area under the curve values, blood glucose and insulin concentrations and increments at each time will be subjected to repeated-measures analysis of variance. After demonstration of significant heterogeneity, the significance of the differences between individual means will be assessed using Tukey's test to adjust for multiple comparisons, with the criterion for significance being two-tailed p\<0.05. Means which differ by more than the least significant difference differ significantly.

Conditions

Interventions

TypeNameDescription
OTHERALLSWEET®ALLSWEET®, is a non-GMO certified allulose developed by the study sponsor. It will be diluted in water.
OTHERALLSWEET® and sucroseALLSWEET®, is a non-GMO certified allulose developed by the study sponsor. It will be added to sucrose (table sugar) and diluted in water.
OTHERSucroseTable sugar. It will be consumed by diluting it in water.

Timeline

Start date
2021-09-15
Primary completion
2021-10-12
Completion
2021-10-28
First posted
2022-01-11
Last updated
2022-01-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05185960. Inclusion in this directory is not an endorsement.