Remote Monitoring impact on cardiac arrhythmia detection in Adults with Implantable Loop Recorders

Not Applicable

Completed

• Conditions: Syncope.; Embolic stroke.; Cardiovascular - Diseases of the vasculature and circulation including the lymphatic system; Cardiovascular - Other cardiovascular diseases; Stroke - Ischaemic

• Registration Number: ACTRN12618001359224
• Lead Sponsor: John Hunter Hospital, Department of Cardiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-08-13
• Study Completion: 2020-02-10
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Participants with standard indications for an implantable loop recorder.

Exclusion Criteria

Pregnant or breastfeeding females.
Inability to provide informed consent.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to first hospital admission, as reported by participants and assessed at final follow-up visit at 12 months.[End of follow-up of 12 months after randomisation.];Frequency of Hospital admission, as reported by participants and assessed at final follow-up visit at 12 months.[End of follow-up of 12 months after randomisation.];Time from randomisation to detection of significant arrhythmia by the ILR (tachycardia or bradycardia clinically likely to cause syncope, or >5.5 minutes of new atrial fibrillation). [End of follow-up of 12 months after randomisation.]