The MagnaSafe Registry: Determining the Risks of Magnetic Resonance Imaging (MRI) in the Presence of Pacemakers and Implantable Cardioverter Defibrillators (ICDs)

Conditions

Implantable Cardioverter Defibrillator Implanted | Need for MRI Imaging With Pacemaker or

What is the purpose of this trial?

This study will create a registry of patients with pacemakers and implantable ICDs who will undergo clinically indicated MRI and will document the incidence of any adverse events or changes in device parameters that might be associated with the procedure.



Participation Guidelines

Age:
18 Years - N/A
Gender:
Both

Click here for detailed information about who can participate in this trial.


Sponsor:
Biotronik, Inc.
Boston Scientific Corporation
Scripps Health
St. Jude Medical
The Hewitt Medical Research Foundation
The Scripps Foundation
Dates:
April 2009
Last Updated:
July 10, 2014
Study HIC#:

Clinicaltrials.gov ID: NCT00907361