Effectiveness of the Eko Digital Stethoscope in Capturing Infant ECGs
NCT06382207
Arrhythmias, Cardiac, Cardiac Conduction System Disease
Richmond, Virginia, United States
View Trial DetailsNCT Number: NCT02933619
Following product approval, confirmation of appropriate VF episode detection after MRI exposure of the ProMRI ICD/CRT-D systems and to evaluate left ventricular pacing threshold changes post-MRI.
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Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Up to 5 years post-approval
Primary objectives will be analyzed once 25 subjects implanted with the ProMRI ICD system have been identified with a documented true VF episode post-MRI.
Time frame: Up to 5 years post-approval
Time frame: Up to 5 years post-approval
Proportion of subjects with appropriate restoration of tachycardia detection and ICD therapy post-MRI.
Time frame: Up to 5 years post-approval
Proportion of subjects who experience left ventricular sensing amplitude attenuation >50% between pre-MRI and 30 days post-MRI.
Looking for future studies?
Notify MeBiotronik, Inc.
Industry
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