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A registry (Patient Data Collection) in Patients with Implantable Cardioverter Defibrillator implant.

Continuous ST Segment Monitoring and Incidence of Clinical Events in ICD Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2009/091/000961
Enrollment
1000
Registered
2010-02-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Heart Failure

Interventions

Intervention1: ICD Implant: Control Intervention1: NIL: NIL

Sponsors

St Jude Medical Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any patient candidate implanted with a St Jude Medical AnalyST or AnalyST Accel DR/VR device, as per current guidelines, can be enrolled in this registry.

Exclusion criteria

Exclusion criteria: Patient not willing or able to understand and sign the Data Transfer Authorization form.

Design outcomes

Primary

MeasureTime frame
1. To identify the population of patients being selected by physicians to be implanted with a St Jude Medical Implantable Cardioverter Defibrillator featuring the ST segment monitoring feature(AnalyST & AnalyST Accel VR/DR devices); 2.document the incidence of ST segment shifts, symptomatic or not, in that population and their possible relationships with clinical events (e.g. cardiac arrhythmias, ICD theray, heart failure hospitalizations).Timepoint: Routine device follow-ups such as 1/3/6/12 Month after implant

Secondary

MeasureTime frame
To document the change in patient management related to availability of device diagnostics.Timepoint: Routine device follow-ups such as 1/3/6/12 Month after implant

Countries

India

Contacts

Public ContactSumit Anand

St . Jude Medical India Pvt Ltd.

sanand@sjm.com918860661364

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026