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Evaluation of Interference Between Cell Phones and Implantable Cardioverter Defibrillators

Evaluation of Interference Between Cell Phones and Implantable Cardioverter Defibrillators

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02330900
Enrollment
54
Registered
2015-01-05
Start date
2014-11-30
Completion date
2015-01-31
Last updated
2016-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electromagnetic Interference

Keywords

Implantable cardioverter defibrillator, Electromagnetic interference, Cell phone

Brief summary

Evaluation of electromagnetic interference between modern cell phones and contemporary implantable cardioverter defibrillators (ICDs)

Detailed description

Electrograms of ICDs will be analyzed during wireless telemetry and during exposure to an activated cell phone. ICD therapy will have been temporarily inactivated before exposure to cell phones to avoid inappropriate shocks, and the sensitivity level of the ICD will be set to maximum. The cell phones will be held over the ICD generator, as well as in the parasternar region (close to the ICD lead, which senses the signals). Interference will be assessed by the presence of visible artefacts on the real-time electrogram, with ICD marker annotations showing atrial and/or ventricular sensed episodes. The outcome measure will be the number and proportion of patients who have electromagnetic interference of the ICD when exposed to cell phones. The procedure will take approximately 5-10minutes, with reprogramming of the device at the end of the test. No further follow-up in the context of the study will be performed.

Interventions

OTHERStudy group

Exposure to cell phone interference of the ICD

Sponsors

University Hospital, Geneva
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Implantation with a wireless-enabled ICD

Exclusion criteria

* Age \<18yrs * inability to sign an informed consent * pacemaker dependancy

Design outcomes

Primary

MeasureTime frameDescription
Number of patients who have electromagnetic interference of the ICD when exposed to cell phones.5-10minutesDetection of electromagnetic interference

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026