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Effect of Empagliflozin on Ventricular Repolarization. (EMPATHYHEART)

U

University of Sao Paulo

Status and phase

Completed
Phase 4

Conditions

Coronary Heart Disease
Arrythmia, Cardiac
Diabetes Mellitus, Type 2

Treatments

Drug: Empagliflozin 25 MG

Study type

Interventional

Funder types

Other

Identifiers

NCT04117763
99613518.9.0000.0068

Details and patient eligibility

About

The present project aims to investigate if the empagliflozin has an antiarrhythmic action. Analyzing the T-wave heterogeneity index, a new electrocardiographic risk marker associated with the prediction of cardiovascular risk, in diabetic patients and coronary artery disease, the investigators will verify if empagliflozin is associated with a reduction in electrical instability.

Full description

Cardiovascular diseases are the leading cause of morbidity and mortality in diabetic patients.

New hypoglycemic drugs are required to undergo cardiovascular safety studies for their release. In 2015, EMPA-REG OUTCOME, which was done for empagliflozin´s approval was the first study to provide evidence that an antidiabetic agent could decrease cardiovascular events. The results demonstrated a reduction in the primary outcome (death by cardiovascular causes, nonfatal infarction, and nonfatal stroke), cardiovascular mortality and hospitalization for heart failure in patients with type 2 diabetes at high cardiovascular risk who received empagliflozin in combination with standard treatment. It is noteworthy that the study population was under-optimized clinical treatment with antihypertensives, statin and aspirin and especially it is noteworthy that the difference in the primary outcome over placebo became evident only three months after treatment´s start.

The potential mechanisms underlying the surprising cardiovascular benefits of empagliflozin are not fully understood.

The present project aims to investigate if the empagliflozin has an antiarrhythmic action. Analyzing the T-wave heterogeneity index, a new electrocardiographic risk marker associated with the prediction of cardiovascular risk, in diabetic patients and coronary artery disease, we will verify if empagliflozin is associated with a reduction in electrical instability.

Enrollment

90 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Age ≥ 18 years;

    • Fasting glycemia> 100 mg/dl or previous diagnosis of type 2 diabetes mellitus;
    • Coronary artery disease, defined by one of the following criteria: the antecedent of myocardial infarction; the evidence of significant coronary stenosis in previous coronary angiography; the noninvasive positive test for ischemia (stress electrocardiogram, stress echocardiogram, stress scintigraphy)
    • TWH ≥ 80 microvolts

Exclusion criteria

  • Chronic renal insufficiency with glomerular filtration rate ≤ 45 ml / min / 1.73m2;
  • Hepatic insufficiency (determined by Child-Pugh, B or C classification);
  • Age ≥ 85 years;
  • 12-lead resting electrocardiogram with the following changes: intraventricular conduction disorders (bundle branch block), pacemaker rhythm, atrial fibrillation or flutter, artifact stroke distortion or baseline fluctuation

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

90 participants in 1 patient group

Empagliflozin
Experimental group
Description:
Empagliflozin 25 mg once daily for 3 months
Treatment:
Drug: Empagliflozin 25 MG

Trial contacts and locations

1

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Central trial contact

Cristiane Lauretti, MD; Bruno Caramelli, MD, PhD

Data sourced from clinicaltrials.gov

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