Remote Monitoring of patients having implantable cardiac devices.
Not Applicable
- Conditions
- Health Condition 1: I259- Chronic ischemic heart disease, unspecifiedHealth Condition 2: I258- Other forms of chronic ischemic heart disease
- Registration Number
- CTRI/2022/02/040509
- Lead Sponsor
- Max Super Speciality Hospital A Unit of Devki Devi Foundation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. All patients implanted with marketed Abbott ICD/CRT/ devices
Exclusion Criteria
1. Patients with life expectancy less than 12 months
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary end point is to compare impact of remote monitoring on early detection <br/ ><br>of adverse events (death, stroke or cardiovascular events requiring surgical intervention or detection of Atrial fibrillation requiring medical intervention/Ablation) between the treatment and control arm. <br/ ><br>Timepoint: 24 months
- Secondary Outcome Measures
Name Time Method Descriptive end point of registry is to compare the impact of remote monitoring on reduction in number of ODP/Clinic and ER visitTimepoint: 24 months