Mortality Analysis of ST Elevation Myocardial Infarction (STEMI) Patients in Belgium

The purpose of this observational study is to assess predictors of in-hospital mortality in patients with acute myocardial infarction admitted to Belgian hospitals.

Completed

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Key information

Conditions

Acute Myocardial Infarction Acute Coronary Syndrome Cardiovascular Diseases Heart Diseases Infarction Ischemia Myocardial Infarction Myocardial Ischemia Necrosis Pathologic Processes Pathological Conditions, Signs and Symptoms Vascular Diseases

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier de Jolimont

La Louvière, Hainaut, 7100, Belgium

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

clinical diagnosis of acute myocardial infarction with ST elevation or left bundle branch blok pattern on ECG

Exclusion criteria

acute myocardial infarction as an acute complication of coronary intervention

Treatment and study plan

Primary outcomes

all cause mortality

Time frame: one month

Sponsors and collaborators

Lead sponsor

Universiteit Antwerpen

Other

Collaborators

Belgian Government

Registry information

Official study title

Prospective Observational Study to Assess Predictors of in Hospital Mortality in STEMI Patients Admitted in Belgian Hospitals

Important dates

Study start: 2007
Primary completion: 2024
Study completion: 2025
First posted: Aug 4, 2008
Registry last updated: Jul 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed