Deactivation of Implantable Cardioverter Defibrillator During Non-thoracic Surgical Procedures
NCT00806377 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2017-05-31
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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