These documents describe an IRB-approved research study and clinical safety workflow that allows patients with pacemakers/ICDs (CIEDs) to undergo clinically indicated MRI with standardized monitoring, device programming, and follow-up, while collecting data to document safety.
The Protocol lays out the study rationale, eligibility, MRI/device management steps, monitoring, outcomes, and data repository plan, and the Consent Form explains the study purpose, what participants will experience, risks/benefits, privacy/data use, costs, and participant rights.
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Publish Date or Last Revised
December 15, 2025
Resource Type
- Best Practices
- Data / Registries
- Guidelines / Clinical Documents
- Workflows
Therapeutic Area
Device Management, Heart Failure
Management
General / Comprehensive Management, Patient Identification, Procedure / Surgery
Setting
Device Care, Electrophysiology Lab, Inpatient, Outpatient
Quality Improvement Topic
Access, Implementation Science, Safety, Technology and Device Management
Related Resources
Best Practices
+ 2 other(s)