Registry intends to prospectively collect data regarding the safety of magnetic resonance imaging (MRI) studies in patients with cardiac pacemakers on implantable cardioverter defibrillators.
Study Type
OBSERVATIONAL
Enrollment
1,000
MRI scan with Specific Absorption Rate (SAR) limit of 1.5 watts per kilogram of body weight
Mayo Clinic
Rochester, Minnesota, United States
Cardiac Implantable Electronic Device Lead Impedance at Different Timepoints
Time frame: Baseline, Visit 1, 3 months, 6 months
Cardiac Implantable Electronic Device Lead Threshold at Different Timepoints
Time frame: Baseline, Visit 1, 3 months, 6 months
P/R Wave Amplitude at Different Timepoints
Time frame: Baseline, Visit 1, 3 months, 6 months
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