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ICD-ON Registry: Periop Management of Cardiac Devices

NCT02052453 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2017-07-28

No results posted yet for this study

Summary

The purpose of this registry is to document incidence of electrical magnetic interference (EMI), change in programmed parameters or device related events in patients with Pacemakers (PM) and Implanted Cardioverter Defibrillators (ICDs) having surgery requiring electrocautery. A standardized perioperative device management protocol (ICD-ON Protocol) will be used.

Conditions

  • Oversensing Cardiac Pacemaker
  • ICD
  • Surgery

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Abbott Medical Devices

    collaborator INDUSTRY

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • Edward Hospital

    lead OTHER

Principal Investigators

  • Janet Gifford, MSN, NP · Edward Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02052453 on ClinicalTrials.gov