Impact of EMpagliflozin on Cardiac Function and Biomarkers of Heart Failure in Patients With Acute MYocardial Infarction

NCT03087773 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 476

Last updated 2024-08-22

Study results available
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Summary

This study is planned to investigate the impact of Empagliflozin on biomarkers of heart failure in patients with myocardial infarction with and without type 2 diabetes mellitus within 6 months after the event.

Conditions

  • Acute Myocardial Infarction

Interventions

DRUG

Empagliflozin 10 mg

The subject will receive Empagliflozin 10 mg orally once daily for 26 weeks.

DRUG

Placebo Oral Tablet

The subject will receive Placebo orally once daily for 26 weeks.

Sponsors & Collaborators

  • United Arab Emirates University

    collaborator OTHER
  • Medical University of Vienna

    collaborator OTHER
  • Landeskrankenhaus Feldkirch

    collaborator OTHER
  • Paracelsus Medical University

    collaborator OTHER
  • Hospital Rudolfstiftung

    collaborator OTHER
  • Klinikum Klagenfurt am Wörthersee

    collaborator OTHER
  • Barmherzige Brüder Eisenstadt

    collaborator OTHER
  • Cardinal Schwarzenberg Hospital

    collaborator OTHER
  • Johannes Kepler University of Linz

    collaborator OTHER
  • Landesklinikum Sankt Polten

    collaborator OTHER
  • Landeskrankenhaus II Graz West

    collaborator OTHER
  • Medical University of Graz

    lead OTHER

Principal Investigators

  • Harald Sourij, Assoc.-Prof. · Medical University of Graz

  • Dirk von Lewinski, Assoc.-Prof. · Medical University of Graz

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-11
Primary Completion
2022-05-03
Completion
2022-05-17

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03087773 on ClinicalTrials.gov