2,039
Participants
Start Date
April 30, 2009
Primary Completion Date
June 30, 2014
Study Completion Date
June 30, 2014
MRI with pacemaker or ICD
The aim of the present protocol is to prospectively determine the adverse event rate of non-thoracic MRI for patients with implanted cardiac devices by collecting pre- and post-MRI device interrogations in a multi-center registry.
Advanced Cardiovascular Imaging, New York
Allegheny General Hospital, Pittsburgh
Abington Health System, Abington
Aventura Hospital and Medical Center, Aventura
University of Mississippi Medical Center, Jackson
Baptist Health Lexington, Lexington
Northern Indiana Research Alliance, Fort Wayne
Providence Heart Institute, Southfield
Aurora St. Luke's Medical Center, Milwaukee
Medical College of Wisconsin, Milwaukee
Oklahoma Heart Research and Education Foundation, Tulsa
The Methodist Hospital, Houston
Intermountain Medical Center, Murray
UCLA Cardiac Arrhythmia Center, Los Angeles
Providence St. Joseph Medical Center, Burbank
Scripps Clinic/Green Hospital, La Jolla
Scripps Memorial Hospital, La Jolla
University of California, San Diego, San Diego
Spectrum Clinical Research, Moreno Valley
Yale University School of Medicine, New Haven
The Valley Hospital, Ridgewood
Collaborators (3)
Scripps Clinic
OTHER
Abbott Medical Devices
INDUSTRY
Boston Scientific Corporation
INDUSTRY
Biotronik, Inc.
INDUSTRY
Scripps Health
OTHER