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Clinical Trial Summary

Patients with implanted pacemaker (PM) or cardioverter-defibrillator (ICD) systems are restrained in daily life by possible electromagnetic interference (EMI). Case reports suggest EMI between PM or ICD systems and hand-held metal detectors that are intensively used as part of security screening processes in e.g. airport controls.

The objective was to determine the safety of screening procedures for ferrous materials with regard to possible in vivo EMI between hand-held metal detectors and PM and ICD systems.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01369706
Study type Interventional
Source Deutsches Herzzentrum Muenchen
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date December 2010

See also
  Status Clinical Trial Phase
Completed NCT02252575 - Assessment of Electromagnetic Interference Between E-transportation and Cardiac Implantable Electronic Devices N/A
Recruiting NCT02349737 - Evaluation of Interference Between Bioelectrical Impedance Analysis and Implantable Cardioverter Defibrillators N/A
Completed NCT02617355 - Interference Between Surgical Magnetic Drapes and Pacemakers N/A
Recruiting NCT02330900 - Evaluation of Interference Between Cell Phones and Implantable Cardioverter Defibrillators N/A
Completed NCT03264222 - Safety of a New Security Device in Patients With Implanted Cardiac Electronic Devices N/A
Completed NCT03508128 - Evaluation of EMI in Patients With Micra Leadless Pacemaker