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Clinical Trials/NCT05050500
NCT05050500
Completed
Phase 4

Effects of Dapagliflozin on Inflammatory Factorslevel and Prognosis in Type 2 Diabetes With Acute Myocardial Infarction

Qingdao Central Hospital1 site in 1 country143 target enrollmentMay 8, 2023

Overview

Phase
Phase 4
Intervention
Dapagliflozin 10mg/Tab
Conditions
Myocardial Infarction
Sponsor
Qingdao Central Hospital
Enrollment
143
Locations
1
Primary Endpoint
MACE events
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

Dapagliflozin is one of the SGLT-2 inhibiters. Recent clinical trials have demonstrated that SGLT-2 inhibitors are effective for treating heart failure. The DAPA-HF clinical trial has demonstrated that the effects of empagliflozin and dapagliflozin improve renal outcomes and reduce all-cause and cardiovascular death in patients with HFrEF[1]. However, its effect on myocardial infarction, the most common disease leading to death in the population, has not been evaluated sufficiently. A meta-analysis has demonstrated that compared with the control, SGLT2 inhibitor is associated with a reduction in the incidence of major adverse cardiovascular events (MACEs), myocardial infarction, cardiovascular mortality and all-cause mortality[2]. It seems that dapagliflozin might be effective for patients with acute myocardial infarction based on these studies. Thus, this study aims to evaluate the effect of dapagliflozin on short-term prognosis in patients with acute myocardial infarction compared to placebo.

  1. Faiez Zannad, João Pedro Ferreira, Stuart J Pocock et el. SGLT2 inhibitors in patients with heart failure with reduced ejection fraction: a meta-analysis of the EMPEROR-Reduced and DAPA-HF trials. Lancet. 2020 Sep 19;396(10254):819-829.
  2. Cai-Yan Zou, Xue-Kui Liu, Yi-Quan Sang et el. Effects of SGLT2 inhibitors on cardiovascular outcomes and mortality in type 2 diabetes: A meta-analysis. Medicine (Baltimore). 2019 Dec;98(49):e18245.
Registry
clinicaltrials.gov
Start Date
May 8, 2023
End Date
December 30, 2024
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with acute MI, either STEMI or NSTEMI, according to the fourth universal definition of MI (Thygesen et al. 2019), disease onset within 7 days.
  • Previously diagnosed with type2 diabetes mellitus, newly diagnosed type2 diabetes according to ADA criteria or glucose intolerance.
  • Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form and the protocol.

Exclusion Criteria

  • Patients diagnosed with Type 1 Diabetes Mellitus.
  • Patients with renal dysfunction. (GFR\<90mmol/L).
  • Patients who have recently undergone immunosuppressive therapy.
  • Patients with a history of recurrent urinary tract infections.
  • Patients who are known to be allergic to SGLT-2 inhibitors.
  • Patients who are hemodynamically unstable.
  • Chronic symptomatic heart failure within the last year and known reduced ejection fraction (LVEF≤40 %), documented before the current MI hospitalization.
  • Severe hepatic impairment (Child-Pugh class C) at the time of inclusion into the trial.
  • Any other non cardiovascular diseases, such as active malignancy requiring treatment at the time of screening or with a life expectancy of fewer than two years based on the investigator´s clinical judgment.
  • Currently on treatment with a sodium-glucose co-transporter 2 inhibitor (SGLT2-inhibitor).

Arms & Interventions

Intervention Group

Dapagliflozin 10 mg every 24 hours for 12 months

Intervention: Dapagliflozin 10mg/Tab

Control Group

AMI standard therapy for 12 months

Intervention: control group

Outcomes

Primary Outcomes

MACE events

Time Frame: 12 months

To assess the occurence of myocardial infarction, stroke and death from cardiovascular causes in post-infarction patients during the follow-up time.

Post-infarction angina

Time Frame: 12 months

Evaluate the post-infarction angina occurence in both groups

IL-6

Time Frame: baseline, 1 month, 3 month, 6 month, 12 month

Serum IL-6 level

The rate of heart failure occurrence

Time Frame: 12 months

Assess the rate of new-onset heart failure during the study follow-up.

Secondary Outcomes

  • IL-1β(baseline, 1 month, 3 month, 6 month, 12 month)
  • hs-CRP(baseline, 1 month, 3 month, 6 month, 12 month)

Study Sites (1)

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