Heart Monitoring Device After Acute Myocardium Infarction

Last updated: April 4, 2019
Sponsor: Instituto de Cardiologia do Rio Grande do Sul
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Coronary Artery Disease

Heart Disease

Congestive Heart Failure

Treatment

N/A

Clinical Study ID

NCT03494751
5391/17
  • Ages > 18
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • patients over 18 years

  • patients post-acute myocardial infarctium

Exclusion

Exclusion Criteria:

  • patients with neurological disease

  • patients with congenital heart disease

Study Design

Total Participants: 358
Study Start date:
May 01, 2019
Estimated Completion Date:
July 01, 2020

Study 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.