ICD-ON Registry: Periop Management of Cardiac Devices

Completed

Conditions studied: Oversensing Cardiac Pacemaker, ICD, Surgery

In brief

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.

Key facts

Study ID

NCT02052453

Run by

Edward Hospital

People needed

350

Starts

2014-02-01

Expected to finish

2015-12-01

Last updated by the study team

2017-07-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Have an ICD from Boston Scientific under Product Advisory related to magnet performance
• Have an ICD or PM from Biotronik or Sorin
• Surgical procedures with two or more electrocautery operators.

Where it is running

• Advocate Good Samaritan Hospital — Downers Grove, Illinois, United States
• Elmhurst Hospital — Elmhurst, Illinois, United States
• Edward Hospital — Naperville, Illinois, United States

Full record on ClinicalTrials.gov

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