Mayo Clinic Cardiac Implantable Electronic Device MRI Registry

NCT02357082 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2022-06-10

No results posted yet for this study

Summary

Registry intends to prospectively collect data regarding the safety of magnetic resonance imaging (MRI) studies in patients with cardiac pacemakers on implantable cardioverter defibrillators.

Conditions

  • Magnetic Resonance Imaging

Interventions

RADIATION

MRI Scan

MRI scan with Specific Absorption Rate (SAR) limit of 1.5 watts per kilogram of body weight

Sponsors & Collaborators

Principal Investigators

  • Paul A Friedman, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2022-04-20
Completion
2022-04-20
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02357082 on ClinicalTrials.gov