MedTrace Logo

Evaluation of EMI in Patients With Micra Leadless Pacemaker

NCT03508128 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2018-08-21

No results posted yet for this study

Summary

Subjects with Medtronic Micra leadless pacemaker who require surgical procedures will have postoperative interrogations reviewed for evidence of electromagnetic interference (EMI).

Conditions

  • Electromagnetic Interference

Interventions

OTHER

surgical procedure

Surgical procedure

Sponsors & Collaborators

  • Edward-Elmhurst Health System

    lead OTHER

Principal Investigators

  • Janet Gifford, MSN · Edward-Elmhurst Health

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-04-04
Primary Completion
2018-08-18
Completion
2018-08-18

Countries

  • United States

Study Locations

More Related Trials

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 NCT03508128 on ClinicalTrials.gov