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

NCT02318550 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 262

Last updated 2021-08-31

Study results available
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Summary

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.

Conditions

  • MRI Scans
  • Magnetic Resonance Imaging
  • Pacemaker
  • Implantable Cardioverter Defibrillator

Interventions

OTHER

MRI Scan

The MRI will be performed with a 1.5 T scanner utilizing institutional protocols and the following settings: * Normal operating mode * SAR ≤ 2.0 W/kg per patient.

Sponsors & Collaborators

  • Lancaster General Hospital

    lead OTHER

Principal Investigators

  • Sandeep Bansal, MD · Lancaster General Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2018-06-30
Completion
2018-06-30

Countries

  • United States

Study Locations

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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 NCT02318550 on ClinicalTrials.gov