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
| Type | Name | Description |
|---|---|---|
| OTHER | ALLSWEET® | ALLSWEET®, is a non-GMO certified allulose developed by the study sponsor. It will be diluted in water. |
| OTHER | ALLSWEET® and sucrose | ALLSWEET®, is a non-GMO certified allulose developed by the study sponsor. It will be added to sucrose (table sugar) and diluted in water. |
| OTHER | Sucrose | Table 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.