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Clinical Trials/NCT06774807
NCT06774807CompletedNot Applicable

Antagonist of the Glucagon-like Peptide 2 (GLP-2) Receptor

University of Copenhagen2 sites in 1 country10 target enrollmentStarted: May 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
2
Primary Endpoint
SMA blood flow

Study Overview

Brief Summary

This project will describe the role of physiological levels of GLP-2 in regulating the blood flow to the intestines and the effect of the antagonist GLP-2(3-33) in blocking these effects of GLP-2.

Detailed Description

Ten healthy participants will meet fasting and attend four randomized experimental days of MRI-scans of the abdomen. Each day will include subcutaneous injections of GLP-2 or saline and intravenous infusion of either the GLP-2 (3-33) antagonist or saline. The infusion start at timepoint -20, while the subcutaneous injection is given to timepoint 0 and the participant will lay in the scanner in one hour after injection. Eight MR-scans are done repeatedly to measure the blood flow in larger abdominal vessels and four blood samples are taken during the experimental day for analysis of GLP-2(1-33), GLP-2(3-33) and bone markers.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age 18-70 years
  • BMI 19-28 kg/m2

Exclusion Criteria

  • Chronic illness that affects the cardiovascular system or gastrointestinal tract
  • Treatment with medicine or supplements that cannot be paused for 12 hours
  • Intake of above 14 alcoholic drinks per week or substance abuse
  • Liver enzymes (ALAT) above 2 times normal values
  • Decreased kidney function (eGFR below 90 or creatinine levels over reference value)
  • Low blood percentage (hemoglobin below reference value)
  • Any condition or disease that the persons responsible for the study find would interfere with the participation of the study.

Outcomes

Primary Outcomes

SMA blood flow

Time Frame: 85 minutes

Blood flow in the superior mesenteric artery

Secondary Outcomes

  • PVblood flow(85 minutes)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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