Registry of Patients for MRI With Non-MRI Conditional Pacemakers and ICD Non-MRI Conditional Pacemakers and ICD

Completed

Conditions studied: MRI Scans, Magnetic Resonance Imaging, Pacemaker, Implantable Cardioverter Defibrillator

In brief

The purpose of the registry is to accumulate pre-and post-scan device interrogation data for the purpose of determining the risk of MRI for patients with implantable devices.

Key facts

Study ID

NCT02318550

Run by

Lancaster General Hospital

People needed

262

Starts

2014-12-01

Expected to finish

2018-06-30

Last updated by the study team

2021-08-31

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Non-device related contraindication for MRI (such as implanted metallic objects, claustrophobia, morbid obesity)
• Presence of capped/abandoned/epicardial leads or subcutaneous coil
• Pregnancy
• Device generator at elective replacement interval
• Abdominal device implant

Where it is running

• Lancaster General Hospital — Lancaster, Pennsylvania, United States

Full record on ClinicalTrials.gov

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