Burden of Remote Monitoring Alerts in Patients with a Cardiac Implantable Electronic Device

Not Applicable

• Conditions: Permanent Pacemaker; Implantable Cardioverter Defibrillator; Implantable Loop Recorder; Cardiac Arrhythmias; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12620000659909
• Lead Sponsor: niversity of Adelaide

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-09
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 26713

Inclusion Criteria

Any patient currently receiving remote monitoring via our remote monitoring system, PaceMate.

Exclusion Criteria

None

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The total number of remote monitoring alerts transmitted via the remote monitoring system, from each of the 3 patient device groups (permanent pacemaker, implantable cardioverter defibrillator, implantable loop recorder,) at the end of a 12-month monitoring period.[12 months]

Secondary Outcome Measures

Name	Time	Method
The number of red alerts (high acuity) transmitted via the remote monitoring system, from each of the 3 device groups (permanent pacemaker, implantable cardioverter defibrillator, implantable loop recorder), at the end of a 12-month monitoring period.[12 months];The number of yellow alerts (lower acuity) transmitted via the remote monitoring system, from each of the 3 device groups (permanent pacemaker, implantable cardioverter defibrillator, implantable loop recorder), at the end of a 12-month monitoring period.[12 months]