Type2 Diabetes Clinical Trial
— SGLTiOfficial title:
The Effects of SGLT Inhibition on Diabetic Cardiomyopathy
Verified date | August 2021 |
Source | The University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Active, not recruiting |
Enrollment | 30 |
Est. completion date | September 30, 2021 |
Est. primary completion date | March 4, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years to 90 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Queen Mary Hospital | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in myocardial perfusion reserve index | Change in myocardial perfusion reserve index calculated from cardiac MRI | 8-12 weeks |
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