Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Obesity
  • Type2 Diabetes
Type
Interventional
Phase
Phase 4
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Prospective Randomised Open Blinded End-point (PROBE) pilot studyMasking: None (Open Label)Primary Purpose: Basic Science

Participation Requirements

Age
Between 18 years and 99 years
Gender
Both males and females

Description

This is a single centre Prospective Randomised Open Blinded End-point (PROBE) pilot study designed to understand the role the GLP-1 receptor agonist, exenatide, and glucagon receptor co-agonism has on normal cardiac physiology, myocardial energetics and myocardial glucose utilisation. Overweight par...

This is a single centre Prospective Randomised Open Blinded End-point (PROBE) pilot study designed to understand the role the GLP-1 receptor agonist, exenatide, and glucagon receptor co-agonism has on normal cardiac physiology, myocardial energetics and myocardial glucose utilisation. Overweight participants with type 2 diabetes will act as their own control and will undergo a series of four imaging visits (in a randomised order) as detailed below: Cardiac positron emission tomography-magnetic resonance imaging (PET-MRI) with carbon-11 acetate (11C-acetate) - placebo infusion Cardiac PET-MRI with fluorine-18-fluorodeoxyglucose (18F-FDG) - placebo infusion Cardiac magnetic resonance imaging (CMR) - placebo infusion. Followed by Cardiac PET-MRI 11C-acetate - exenatide and glucagon infusion. Followed by CMR - exenatide and glucagon infusion Cardiac PET-MRI with 18F-FDG - exenatide and glucagon infusion Study outcome measures are detailed below

Tracking Information

NCT #
NCT04307797
Collaborators
Antaros Medical AB
Investigators
Principal Investigator: Ian Wilkinson, MD University of Cambridge