Does Paracetamol Influence the Release of Gut Hormones, Glucose Absorption and Glycemia?

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Copenhagen

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 volunteers

Qualifiers

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

Design model

Crossover

Treatments tested in this trial

  • Paracetamol

    Other intervention

    Paracetamol is used as a tool to block prostaglandin synthesis

  • Placebo

    Other intervention

    A placebo will be administered to be able to determine the effect of paracetamol on prostaglandin synthesis

Treatment groups

12 Participants
are divided into 2 treatment groups
Group A: Paracetamol (1000mg)Active comparator 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Glucagon-like peptide 1

Plasma concentration

Time frame
From baseline samples (-15, 0 min) until the end of the meal test at t = 180min

Secondary outcomes

1

Glucose

Plasma concentration

Time frame
From baseline samples (-15, 0 min) until the end of the meal test at t = 180min
2

Gastrin

Plasma concentration

Time frame
From baseline samples (-15, 0 min) until the end of the meal test at t = 180min
3

Cholecystokinin

Plasma concentration

Time frame
From baseline samples (-15, 0 min) until the end of the meal test at t = 180min
4

Glucose-dependent insulinotropic polypeptide (GIP)

Plasma concentration

Time frame
From baseline samples (-15, 0 min) until the end of the meal test at t = 180min

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Copenhagen

Lead sponsor

Hvidovre University Hospital

Collaborator