Clinical Trials Directory

Trials / Completed

CompletedNCT06515340

Effect of Allulose on Diet-induced Thermogenesis

Effect of Allulose on Diet-induced Thermogenesis, Substrate Oxidation, Glycemic Response, and Satiety in Normal Weight Adults

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
11 (actual)
Sponsor
Toronto Metropolitan University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to investigate the dose-response effect of allulose on diet-induced thermogenesis, substrate oxidation, glycemic response, and subjective appetite in healthy normal weight adults.

Detailed description

A within-subject, repeated measures, randomized, repeated measures design will be used. Participants (n= 10, 5 males, 5 females) will consume, in a random order, one of three varying doses of test treatments (allulose (5g), allulose (10g) or allulose (20g)) on 3 separate days. After treatment consumption, energy expenditure measurements via indirect calorimetry will be collected in 30-min interval (30-min measurement, 30-min rest) for 3 hours. Blood glucose will be measured at baseline and continuously for 3 hours via the Dexcom G6 continuous glucose monitoring system. Subjective appetite (hunger, fullness, desire to eat, prospective food consumption) will be measured via visual analogue scales at baseline and at the end of each energy expenditure measurement interval over 3 hours.

Conditions

Interventions

TypeNameDescription
OTHERAllulose Dose 15 gram consumed orally
OTHERAllulose Dose 210 gram consumed orally
OTHERAllulose Dose 320 gram consumed orally

Timeline

Start date
2024-07-15
Primary completion
2025-03-24
Completion
2025-03-24
First posted
2024-07-23
Last updated
2025-11-17

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06515340. Inclusion in this directory is not an endorsement.