About this trial
The study aim is to determine whether acute inhibition of endogenous prostaglandin synthesis by paracetamol affects the release of gut hormones, glucose absorption and glycemia in healthy young individuals
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age ≥ 18 years
Nondiabetic fasting plasma glucose (< 7.0 mmol/L) at time of inclusion
BMI of 20-25
Written informed consent
Disqualifiers
Haemoglobin < 7.9 mmol/L
Pregnancy or breastfeeding
Significant gastrointestinal symptoms (e.g. dyspepsia, postprandial pain)
Use of medication that cannot be paused for 12 hours or any drug that affects gastric emptying, small intestinal motility, glucose absorption.
Trial design
Crossover
Treatments tested in this trial
Paracetamol
Other interventionParacetamol is used as a tool to block prostaglandin synthesis
Placebo
Other interventionA placebo will be administered to be able to determine the effect of paracetamol on prostaglandin synthesis
Treatment groups
Trial outcomes
Primary outcomes
Glucagon-like peptide 1
Plasma concentration
Secondary outcomes
Glucose
Plasma concentration
Gastrin
Plasma concentration
Cholecystokinin
Plasma concentration
Glucose-dependent insulinotropic polypeptide (GIP)
Plasma concentration
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Copenhagen
Lead sponsor
Hvidovre University Hospital
Collaborator