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Impact on Patient Outcome of Cardiac Implantable Electronic Device Complications (POINTED)

A

Azienda Ospedaliera Cardinale G. Panico

Status

Completed

Conditions

Cardiac Implantable Electronic Device Complications

Treatments

Device: Implantation of a cardiac implantable electronic device

Study type

Observational

Funder types

Other

Identifiers

NCT03612635
POINTED

Details and patient eligibility

About

The purpose of this registry is to evaluate the impact on patient outcome and on healthcare utilization of cardiac implantation electronic device complications during a long-term follow-up.

Full description

Multicentric, observational, prospective registry enrolling consecutive patients underwent pacemaker or defibrillator implantation, aimed to evaluate the impact of cardiac implantable device complications requiring surgical revision on healthcare utilization (number and length of hospitalizations), and on patient outcome (all-cause mortality and cardiac mortality), during a long-term follow-up.

Enrollment

2,811 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients underwent cardiac implantable electronic device implantation according to current guidelines during the enrollment period.

Exclusion criteria

  • patients already carriers of a cardiac implantable electronic device underwent replacement or upgrading of device.

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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