Patient Registry Of Magnetic Resonance Imaging in Non-Approved DEvices — PROMeNADe  

Magnetic Field Exposure Clinical Trial

Official title: Patient Registry Of Magnetic Resonance Imaging in Non-Approved DEvices

Status Completed

Clinical Trial Summary

The investigators are providing MRI in patients with non-MRI approved CIED's (Cardiac Implanted Electronic Devices)

Clinical Trial Description

At Saint Luke's Hospital, despite growing evidence to the contrary, there is extremely limited data and experience with performing MRIs on patient with abandoned and epicardial leads in patients with non-approved ICDs and PMs. There is a limited mechanism to discuss this issue with the patient, screen the patient and assess their device beforehand, monitor them during the MRI examination, keep track of pulse sequences used, assess their devices after (and if necessary, resume prior programming before any changes), and to maintain that experience. The objective of this study is to create a protocol for an MRI at the commonly used magnetic strength of 1.5 T in patients that do not have conditional pacemakers and/or defibrillators and have abandoned or epicardial leads and maintain a registry of participants, devices involved, MRI examinations and pulse sequences used, and to keep records of any follow up events. ;

Related Conditions & MeSH terms

• Magnetic Field Exposure

• NCT number: NCT03081364
• Study type: Observational [Patient Registry]
• Source: Saint Luke's Health System
• Status: Completed
• Start date: September 2015
• Completion date: September 2022