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Study identifier: NCT07463495 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Metabolic Effects of Oral Tributyrin Administration

Condition: Healthy Overweight/Obese  ·  Sponsor: University of Aarhus

PhaseNA
Planned participants12
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this double-blinded randomized clinical cross-over trial is to investigate the metabolic and appetite regulating effects of oral tributyrin (a butyrate pro-drug) administration vs placebo. The main questions it aims to answer are: * Does tributyrin have glucose lowering properties in humans? * Does tributyrin reduce appetite in humans? A sample size calculation estimated a minimum of 10 participants. We expect to include 12 participants in this study. Tributyrin or placebo is ingested once or twice daily for 2x2 weeks, separated by a washout period of minimum 2 weeks. On trial day following each 2-week period we assess: * Postprandial blood sugar levels * Hunger sensations (questionnaire) * Enteroendocrine hormone secretion (GLP-1, GIP, PYY, LEAP2, ghrelin) * Cardiac function (echocardiography) - An exploratory study evaluating the hemodynamic effects assessed by echocardiography is anticipated to be published separately. * Caloric intake (ad libitum meal test) * Gastric emptying rate (acetaminophen test) * Resting metabolic rate (indirect calorimetry). While at home, subjects will wear a sleep monitoring device for three consecutive nights and deliver fecal samples for analysis of short-chain fatty acid content and microbiota composition.

This description comes directly from the study's public registry record.

Talk to the study team

Simon M Denning, MD  ·  0045 78450000  ·  simon.denning@clin.au.dk

Always discuss trial participation with your own doctor first.

Locations (1)

SDCA / Medical Research LaboratoryAarhus N, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT07463495