Deactivation of Implantable Cardioverter Defibrillator During Non-thoracic Surgical Procedures

NCT00806377 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2017-05-31

No results posted yet for this study

Summary

The purpose of this study is:

* To document the incidence of electromagnetic oversensing of ICDs during non-thoracic surgery.
* To identify any non-thoracic procedure with a higher incidence of generating electromagnetic oversensing.
* To document the ability of dual chamber ICDs to discriminate electromagnetic oversensing.

Conditions

  • Implantable Cardioverter-Defibrillators

Sponsors & Collaborators

  • Minneapolis Heart Institute Foundation

    lead OTHER

Principal Investigators

  • William T Katsyiannis, MD · Minneapolis Heart Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2011-10-31
Completion
2011-10-31

Countries

  • United States

Study Locations

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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 NCT00806377 on ClinicalTrials.gov