I-TREAT: Intensive Follow-up via Remote Monitoring for Implantable Cardiac Devices
Not Applicable
Completed
- Conditions
- Heart arrythmiasHeart rhythm disorderCardiovascular - Other cardiovascular diseases
- Registration Number
- ACTRN12621001275853
- Lead Sponsor
- Centre for Heart Rhythm Disorders, University of Adelaide
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
This study will enrol devices across different brands including Biotronik, Boston Scientific, Medtronic and Abbott.
The only inclusion criteria is the device is on PaceMate (vendor neutral remote monitoring system).
The standard of care group will consist of 70 patients, randomly selected from the large cohort of patients who receive standard monitoring. Participants will be matched by age, gender and device type to those patients in the intensive remote-monitoring group.
Exclusion Criteria
Sorin devices on home monitoring as they are not on PaceMate
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method