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Completed No phase listed Observational

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

ClinicalTrials.gov ID: NCT00907361

Public ClinicalTrials.gov record NCT00907361. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 7:52 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The MagnaSafe Registry: Determining the Risks of MRI in the Presence of Pacemakers and Implantable Cardioverter Defibrillators

Study identification

NCT ID
NCT00907361
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Scripps Health
Other
Enrollment
2,039 participants

Conditions and interventions

Interventions

  • MRI with pacemaker or ICD Device

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2009
Primary completion
May 31, 2014
Completion
May 31, 2014
Last update posted
Nov 22, 2015

2009 – 2014

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Providence St. Joseph Medical Center Burbank California 91505
Scripps Clinic/Green Hospital La Jolla California 92037
Scripps Memorial Hospital La Jolla California 92037
UCLA Cardiac Arrhythmia Center Los Angeles California 90095
Spectrum Clinical Research Moreno Valley California 92553
University of California, San Diego San Diego California 92103
Yale University School of Medicine New Haven Connecticut 06520
Aventura Hospital and Medical Center Aventura Florida 33180
Northern Indiana Research Alliance Fort Wayne Indiana 46804
Baptist Health Lexington Lexington Kentucky 40503
Providence Heart Institute Southfield Michigan 48075
University of Mississippi Medical Center Jackson Mississippi 39216
The Valley Hospital Ridgewood New Jersey 07450
Advanced Cardiovascular Imaging New York New York 10128
Oklahoma Heart Research and Education Foundation Tulsa Oklahoma 74133
Abington Health System Abington Pennsylvania 19001
Allegheny General Hospital Pittsburgh Pennsylvania 15212
The Methodist Hospital Houston Texas 77030
Intermountain Medical Center Murray Utah 84157
Aurora St. Luke's Medical Center Milwaukee Wisconsin 53215
Medical College of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00907361, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 22, 2015 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00907361 live on ClinicalTrials.gov.

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