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NCT02052453 · ClinicalTrials.gov registry record

ICD-ON Registry: Periop Management of Cardiac Devices

A clinical trial of Surgery and ICD, sponsored by Edward Hospital.

Completed
Registry status
350
Enrollment target
3
Study locations

NCT02052453 is a study of Surgery and ICD that has completed, run by Edward Hospital. The registered enrollment target is 350 participants, below the 52,849-participant average among 120 other Surgery trials with a reported enrollment target (99% lower). The trial reports 3 study locations across 1 state.

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The verdict

NCT02052453, a study of Surgery and ICD, has completed, sponsored by Edward Hospital.

COMPLETED
Registry status
350 participants
Enrollment target
3
Study locations

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 Studied

Surgery ICD Oversensing Cardiac Pacemaker

Study Locations (3)

Illinois

  • Advocate Good Samaritan Hospital - Downers Grove
  • Elmhurst Hospital - Elmhurst
  • Edward Hospital - Naperville

Trial Details

FieldValue
Enrollment Target 350 participants
Start Date 2014-02
Est. Completion 2015-12

Sponsor

Edward Hospital

4 total trials

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What the Registry Record Tells You About NCT02052453

The ClinicalTrials.gov registry entry for NCT02052453 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 52,849-participant average among 120 other Surgery trials with a reported enrollment target (99% lower). The listed sponsor is Edward Hospital, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 0 interventions.

NCT02052453 reports 3 study locations spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT02052453 about?

NCT02052453 is a clinical study titled "ICD-ON Registry: Periop Management of Cardiac Devices". 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 perioper...

What is the current status of trial NCT02052453?

This trial is currently completed. The enrollment target is 350 participants. The study started on 2014-02. Estimated completion is 2015-12.

What conditions does trial NCT02052453 study?

This clinical trial studies the following conditions: Surgery, ICD, Oversensing Cardiac Pacemaker.

Who is sponsoring clinical trial NCT02052453?

This trial is sponsored by Edward Hospital, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02052453 being conducted?

This trial has 3 study locations across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.