Last updated on August 2015

European Health Economic Trial on Home Monitoring in ICD and CRT-D Patients (EuroEco)


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Ventricular Fibrillation | Tachycardia | Ventricular Flutter | Ventricular
  • Age: Between 18 - 100 Years
  • Gender: Male or Female
  • Other:
    ICD Patient Population - Inclusion Criteria
    Indication for 1-/2- chamber ICD implantation, including replacement indication
    Patient is willing and able to comply with the clinical investigation plan and has
    provided written informed consent
    ICD Patient Population - Exclusion Criteria
    Patients with contraindication to ICD implantation
    Patients with indication for cardiac resynchronization (CRT)
    Minors and pregnant women
    Patients participating in another study
    CRT-D Patient Population - Inclusion Criteria
    Patients with indication for de novo CRT-D implantation according to current
    guidelines
    Patient is willing and able to comply with the clinical investigation plan and has
    provided written informed consent
    CRT-D Patient Population - Exclusion Criteria
    Patients who had a cardiac device implanted before (upgrade, device replacement)
    Life expectancy less than 12 months
    Planned heart transplantation
    NYHA IV
    Minors < 18 years
    Pregnant and breast-feeding women
    Participation in another clinical study

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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