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Heart Monitoring Device After Acute Myocardium Infarction

Not Applicable
Conditions
Acute Myocardial Infarction
Interventions
Device: No heart monitor
Device: Heart monitor
Registration Number
NCT03494751
Lead Sponsor
Instituto de Cardiologia do Rio Grande do Sul
Brief Summary

Verify the effectiveness of a Heart Monitor in preventing events in patients over 18 years after acute myocardial infarction in a clinical unit. Patients with neurological disease or congenital heart disease we excluded from the study.

Detailed Description

Heart Monitor can detect early intercurrences. Objective: To verify the effectiveness of a Heart Monitoring system in preventing events in patients after acute myocardial infarction. Methodology: This is a randomized clinical trial to be developed in a clinical unit and will include patients over 18 years , post-acute myocardial infarction who were transferred from the ICU emergency or hemodynamic to clinical unit. Patients with neurological disease or congenital heart disease will be excluded from the study.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
358
Inclusion Criteria
  • patients over 18 years
  • patients post-acute myocardial infarctium
Exclusion Criteria
  • patients with neurological disease
  • patients with congenital heart disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
No Heart MonitorNo heart monitorNo heart monitor device in the patients with myocardial infarction (control).
Heart MonitorHeart monitorWe used the device (heart monitor) in the patients with myocardial infarction.
Primary Outcome Measures
NameTimeMethod
Heart rhythm monitoringOne year

Evaluating the effectiveness of a heart monitoring device in the prevention and detection of events in patients after acute myocardial infarction

Secondary Outcome Measures
NameTimeMethod
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