Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT04591639

The DAPA-MEMRI Trial

Led by University of Edinburgh · Updated on 2025-06-24

160

Participants Needed

1

Research Sites

414 weeks

Total Duration

On this page

Sponsors

U

University of Edinburgh

Lead Sponsor

A

AstraZeneca

Collaborating Sponsor

AI-Summary

What this Trial Is About

Diabetes mellitus is among the top 10 causes of death worldwide with an increasing incidence. Patients with diabetes are at risk of developing heart failure which is characterised by significant changes in the heart muscle including scarring and thickening. Contraction of the heart involves movement of calcium across the heart muscle and disruption of this process is an early change seen in heart failure. Recently, a drug therapy (SGLT2 inhibitor therapy) in patients with diabetes was shown to benefit patients with heart failure but the mechanisms of benefit are unknown. Our hypothesis is that calcium handling is altered in patients with either type 2 diabetes mellitus (T2DM) or heart failure and that SGLT2 inhibitors can improve this in heart failure irrespective of the presence of T2DM. Scanning the heart using magnetic resonance imaging (MRI) enables detailed assessment of its structure and function by using a new contrast 'dye' containing manganese that has shown advantages over traditional contrast. We plan to further test this new dye as it has the potential to track and quantify improvements in heart function over time and detect changes in calcium handling in the heart muscle, making it an ideal measure to identify the mechanisms of benefit from SGLT2 inhibitor therapy. The study population will comprise patients with heart failure with and without type 2 diabetes, patients with type 2 diabetes without heart failure and healthy volunteers. Baseline comparisons will be made between the four groups before progressing to the randomised controlled trial with heart failure patients only. Patients will have a clinical assessment and blood tests, electrocardiogram, echocardiogram and MRI of the heart at each visit. If successful, this study will give us significant insights into mechanisms of action of SGLT2 inhibitors in heart failure and will enable us to tailor specific treatments in heart failure patients.

CONDITIONS

Official Title

The DAPA-MEMRI Trial

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with heart failure (with or without type 2 diabetes mellitus)
  • Aged over 18 years
  • Diagnosis of symptomatic reduced ejection fraction heart failure for at least 2 months
  • Left ventricular ejection fraction 40% or less
  • Elevated N-terminal pro B-type natriuretic peptide (>125 pg/mL)
  • Clinical diagnosis of type 2 diabetes mellitus for 50% of patient population, on stable therapy for at least 12 months or more
  • Patients with type 2 diabetes mellitus and no heart failure
  • Aged over 18 years
  • Clinical diagnosis of type 2 diabetes mellitus (diagnosed by HbA1c of 48 mmol/mol (6.5%) or greater or fasting plasma glucose level of 7 mmol/L or greater at diagnosis)
  • On stable therapy for at least 12 months or more
  • Normal left ventricular systolic ejection fraction
  • Healthy volunteers
  • Aged over 18 years
  • Normal left ventricular ejection fraction and normal blood sugar
  • No clinically significant co-morbid conditions
Not Eligible

You will not qualify if you...

  • Receiving an SGLT2 inhibitor within 8 weeks of enrolment
  • Previous intolerance of, or contraindication to, an SGLT2 inhibitor
  • Standard magnetic resonance imaging safety exclusions
  • Severe renal impairment (eGFR less than 30 millilitre/min per 1.73 m2) for heart failure patients
  • Type 1 diabetes mellitus
  • Symptomatic low blood pressure or systolic blood pressure less than 95 mmHg
  • Recent (within 12 weeks) hospitalisation for heart failure, acute cardiovascular event (myocardial infarction or stroke) or coronary re-vascularisation
  • 2nd or 3rd degree atrioventricular block
  • Atrial fibrillation or flutter with poor ventricular rate control (over 100/min)
  • Heart failure due to restrictive cardiomyopathy, active myocarditis, constrictive pericarditis, hypertrophic (obstructive) cardiomyopathy or uncorrected primary valvular disease
  • New York Heart Association grade IV heart failure
  • Obstructive liver function testing abnormalities
  • Concomitant digoxin, diltiazem or verapamil therapy
  • Other major clinically significant co-morbid conditions for type 2 diabetes without heart failure
  • History or signs of ischemic heart disease for type 2 diabetes without heart failure
  • Moderate or severe renal impairment (eGFR less than 45 mL/min per 1.73 m2) for type 2 diabetes without heart failure and healthy volunteers
  • Receiving a SGLT2 inhibitor at any time for type 2 diabetes without heart failure and healthy volunteers
  • Abnormal electrocardiogram
  • Clinically significant abnormalities in blood tests
  • Major or clinically significant cardiovascular disease for healthy volunteers
  • Diabetes mellitus for healthy volunteers
  • Symptomatic low blood pressure or systolic blood pressure less than 95 mmHg for type 2 diabetes without heart failure and healthy volunteers

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Edinburgh

Edinburgh, Scotland, United Kingdom

Actively Recruiting

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Research Team

S

Shruti Joshi, MBBS, MRCP

CONTACT

D

David Newby, PhD, BM, DM, MRCP, DSc, FRSE

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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