Arrhythmias in Post-Myocardial Infarction Patients

NCT03231826 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 445

Last updated 2025-08-12

No results posted yet for this study

Summary

Patients are screened for significant arrhythmias and other possibly significant ECG-patterns directly after discharge and two weeks after myocardial infarction using wearable devices. The home monitoring data will be linked with extensive data from electronic health records collected before, during hospital stay and after discharge.

The purpose of the study is to clarify whether home monitoring of continuous ECG-signals can be used to predict and prevent serious adverse events after myocardial infarction.

Conditions

Sponsors & Collaborators

  • Tays Heart Hospital

    collaborator UNKNOWN
  • GE Healthcare Finland Ltd

    collaborator UNKNOWN
  • Fimlab Ltd

    collaborator UNKNOWN
  • VTT Technical Research Centre of Finland

    collaborator OTHER
  • Bittium Ltd

    collaborator UNKNOWN
  • Tekes - Finnish Funding Agency for Innovation

    collaborator UNKNOWN
  • Politecnico Milano

    collaborator UNKNOWN
  • Tampere University

    lead OTHER

Principal Investigators

  • Jussi A Hernesniemi, MD PhD · Tays Heart Hospital and Tampere University

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-22
Primary Completion
2019-02-28
Completion
2019-02-28

Countries

  • Finland

Study Locations

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Entities

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 NCT03231826 on ClinicalTrials.gov