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Clinical Trial Summary

Patients with implanted cardiac devices who meet appropriate entrance criteria undergo clinically indicated Magnetic Resonance (MR) Imaging Studies using an established safety protocol.


Clinical Trial Description

This prospective cohort study to use an established MRI device safety protocol to decrease the risk of clinically indicated MR imaging in patients with implantable cardiac devices. All devices will undergo a complete interrogation and testing of thresholds, sensing, battery voltage and impedances prior to and following imaging. Pre-MRI, devices will be programmed to setting that will ensure MRI safety. During imaging, patients will blood pressure, heart rate and O2 sat level will be monitored continuously. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01130896
Study type Observational
Source Johns Hopkins University
Contact
Status Completed
Phase
Start date May 2003
Completion date January 22, 2015

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