Heart Monitoring Device After Acute Myocardium Infarction
- Conditions
- Acute Myocardial Infarction
- Interventions
- Device: No heart monitorDevice: 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
- patients over 18 years
- patients post-acute myocardial infarctium
- patients with neurological disease
- patients with congenital heart disease
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description No Heart Monitor No heart monitor No heart monitor device in the patients with myocardial infarction (control). Heart Monitor Heart monitor We used the device (heart monitor) in the patients with myocardial infarction.
- Primary Outcome Measures
Name Time Method Heart rhythm monitoring One 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
Name Time Method