The Effects of SGLTi on Diabetic Cardiomyopathy (SGLTi)
Primary Purpose
Type2 Diabetes, Heart Failure With Reduced Ejection Fraction
Status
Unknown status
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
Dapagliflozin
Sponsored by
About this trial
This is an interventional treatment trial for Type2 Diabetes
Eligibility Criteria
Inclusion Criteria:
- type 2 diabetes
- 40-90 years old
- HbA1c >= 6.5%
- history of heart failure with reduced ejection fraction
- indications for SGLT inhibition on clinical ground
Exclusion Criteria:
- angina pectoris or chest discomfort
- prior coronary artery bypass grafts
- coronary artery stenting within 6 months of study enrolment
- pervious myocardial infarct
- any contraindication for stress CMR testing
- renal impairment with eGFR <45ml/min/1.73m2
- limited life expectancy <5 years, for example due to pulmonary disease, cancer or
- significant hepatic failure
- contraindication to dapagliflozin or other SGLT2 inhibitors
- unable to take dapagliflozin
- patients currently on and SGLT2 inhibitor
- planned need for concomitant cardiac surgery or coronary intervention
- refusal or inability to sign an informed consent
- potential for on-compliance towards the requirements in the trial protocol (especially the medical treatment) or follow-up visits
Sites / Locations
- Queen Mary Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Dapagliflozin
Arm Description
Dapagliflozin, one of the SGLT-2 inhibitors, will be prescribed to DM patients on clinical ground
Outcomes
Primary Outcome Measures
Change in myocardial perfusion reserve index
Change in myocardial perfusion reserve index calculated from cardiac MRI
Secondary Outcome Measures
Full Information
NCT ID
NCT04200586
First Posted
December 12, 2019
Last Updated
August 2, 2021
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04200586
Brief Title
The Effects of SGLTi on Diabetic Cardiomyopathy
Acronym
SGLTi
Official Title
The Effects of SGLT Inhibition on Diabetic Cardiomyopathy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 9, 2020 (Actual)
Primary Completion Date
March 4, 2021 (Actual)
Study Completion Date
September 30, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Diabetic cardiomyopathy is associated with significant morbidity and mortality. It is considered as a cardiac muscle disorder secondary to diabetes mellitus (DM). Certain studies show the clinical benefit of SGLT-s inhibitors on reducing cardiovascular outcomes amongst patients with type II DM that go beyond the correction of hyperglycemic perse. Thus an observational imaging study is proposed to identify mechanistic insights of the drug group over cardiovascular events.
Detailed Description
Diabetic cardiomyopathy is defined as ventricular dysfunction in diabetic patients in the absence of coronary artery disease and hypertension. It is considered as a cardiac muscle disorder due to the metabolic consequences of DM characterized by left ventricular hypertrophy, left ventricular diastolic dysfunction (in the early stage), and/or systolic dysfunction. To date, there is no specific treatment proven effective for the condition due to the incomplete understanding of the pathogenesis.
Recent studies however prove the efficacy of SGLT-2 inhibitors on reducing the primary composite end point of cardiovascular outcomes including hospitalization for heart failure, cardiovascular death, and all-cause death amongst patients with type II DM. Such clinical benefit is apparently mainly stemmed from the reduction in heart failure related mortality and sudden cardiac death rather than the macro-vascular events such as myocardial infarct and stroke, suggesting addition benefits going beyond the correction of hyperglycemia perse. These studies thus raise the possibility that the drug may have direct effects on the myocardium that conferring the clinical benefit not related the modification of traditional risk factors such as glycemic control, lipid, blood pressure, and obesity.
A single-arm, observational cardiac magnetic resonance imaging study is proposed in type II diabetic patients before and 2 months after initiation of dapagliflozin. The aim is to identify mechanistic insights leading to the unexpected clinical benefit of SGLT inhibition.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes, Heart Failure With Reduced Ejection Fraction
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Model Description
Single-arm, observational
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Dapagliflozin
Arm Type
Experimental
Arm Description
Dapagliflozin, one of the SGLT-2 inhibitors, will be prescribed to DM patients on clinical ground
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin
Intervention Description
Dapagliflozin, one of the SGLT-2 inhibitors, will be prescribed to DM patients on clinical ground.
Primary Outcome Measure Information:
Title
Change in myocardial perfusion reserve index
Description
Change in myocardial perfusion reserve index calculated from cardiac MRI
Time Frame
8-12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
type 2 diabetes
40-90 years old
HbA1c >= 6.5%
history of heart failure with reduced ejection fraction
indications for SGLT inhibition on clinical ground
Exclusion Criteria:
angina pectoris or chest discomfort
prior coronary artery bypass grafts
coronary artery stenting within 6 months of study enrolment
pervious myocardial infarct
any contraindication for stress CMR testing
renal impairment with eGFR <45ml/min/1.73m2
limited life expectancy <5 years, for example due to pulmonary disease, cancer or
significant hepatic failure
contraindication to dapagliflozin or other SGLT2 inhibitors
unable to take dapagliflozin
patients currently on and SGLT2 inhibitor
planned need for concomitant cardiac surgery or coronary intervention
refusal or inability to sign an informed consent
potential for on-compliance towards the requirements in the trial protocol (especially the medical treatment) or follow-up visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Chung-Wah SIU, Prof
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
12. IPD Sharing Statement
Learn more about this trial
The Effects of SGLTi on Diabetic Cardiomyopathy
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