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NCT07194772: NARELO

Sucralose and Glucose Metabolism in Young Healthy Adults

Completed NA Last updated 26 September 2025
What this trial tests

NA trial testing Low-calorie sweeteners (LCS) in Glucose Intolerance in 42 participants. Completed in 12 June 2024.

Timeline
16 March 2022
Primary endpoint
12 June 2024
12 June 2024

Quick facts

Lead sponsorUniversity of Ottawa
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment42
Start date16 March 2022
Primary completion12 June 2024
Estimated completion12 June 2024
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

University of Ottawa

Who can join

Adults 18 to 35, any sex, with Glucose Intolerance or Glucose and Insulin Response. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aimed to investigate the effects of a three-week consumption of sucralose-sweetened beverages (low-calorie sweetener) on postprandial glycemic responses in healthy adults, compared with sugar-sweetened beverages under real-world conditions. In brief, postprandial glycemic responses are used as an indicator of how your body manages blood sugar levels after consuming glucose. To explore potential mechanisms underlying any observed changes in postprandial glycemic responses, we further investigated potential alterations in gut microbiota composition and functionality, as well as plasmatic biomarkers of intestinal permeability and systemic low-grade inflammation. Finally, this project explored whether free sugars derived from a natural source (100% natural fruit juice) elicit metabolic responses that differ from those of refined sugars. Participants visited the laboratory for a preliminary screening session to assess eligibility prior to being randomly assigned to one of the three experimental groups consuming either sucralose-sweetened beverages (LCS), sucrose-sweetened beverages (SSB), or 100% natural fruit juice (FJ) at dosage approximating real-world consumption over three weeks. Participants underwent two experimental sessions (duration of 3 hours each) at the beginning and completion of the study as outlined below.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Glucose Intolerance

Currently open trials in the same condition.

Other University of Ottawa trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing