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Heart Monitoring Device After Acute Myocardium Infarction

NCT03494751 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 358

Last updated 2019-04-08

No results posted yet for this 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.

Conditions

  • Acute Myocardial Infarction

Interventions

DEVICE

Heart monitor

Use of heart monitor device in the patients after acute myocardium infarct.

DEVICE

No heart monitor

Standard monitoring by nurses.

Sponsors & Collaborators

  • Instituto de Cardiologia do Rio Grande do Sul

    lead OTHER

Principal Investigators

  • silvia goldmeier · Instituto de Cardiologia do Rio Grande do Sul

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-01
Primary Completion
2019-09-01
Completion
2020-07-01

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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 NCT03494751 on ClinicalTrials.gov