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Examination of Implant´s Safety in an Electronic and Magnetic Field Environment

Study of Provocation Concerning Implants´Safety in Electronic and Magnetic Fields in Their Environment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01626261
Acronym
FEMU
Enrollment
281
Registered
2012-06-22
Start date
2009-09-30
Completion date
2018-06-30
Last updated
2018-06-15

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

Conditions

Cardiac Arrhythmia, Disorder of Cardiac Pacemaker System, Disorder of Implantable Defibrillator

Brief summary

The number of active electrical cardiac implants such as internal cardioverter defibrillators (ICDs), pacemakers or cardiac contractility modules (CCM) has significantly risen over the last two decades. This has been paralleled by an increase in the number of sources of electromagnetic fields in daily life and occupational circumstances. To date it remains unclear whether patients are at risk of device failure when being subjected to these fields. There are currently no general guidelines available to help clinicians informing their patients about safety levels and behavior around these electromagnetic fields. This study aims to identify the thresholds of safe use of these devices and potential failures under worst-case conditions in 50/60 Hz fields (i.e. power line frequency). Device implanted patients will be exposed to electric, magnetic and combined fields of different intensity at various device programming (e.g. nominal and maximum sensitivity). The results will show whether patients are safe in public or occupational environments, which medical relevant disturbances can occur and if a correlation exists between disturbances and device type or patients physique.

Interventions

DEVICEMagnetic and electric field´s impact on the implant

Examination of magnetic and electric field's impact on the implant regarding: stability detection threshold using different strength of magnetic and electric field

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* men and women between 18 and 80 years * Implantation of a Pacemaker (SM)-/ ICD-assembly at least four weeks ago * signed informed consent

Exclusion criteria

* enduring addiction of implant * thyroid disease * electrolyte imbalance on the trial day * pregnancy and breastfeeding * acute myocardial infarction (\<30 days) * Comorbidity, which complicates an emergency assistance, e.g. morbus bechterew, glaucoma, micturition disturbance

Design outcomes

Primary

MeasureTime frame
Interference threshold of the device in electromagnetic fields in V/m and/or µTfor every patient during one ambulant visit about 1 hour study examination

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026