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Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-approval Study

NCT02849769 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10979

Last updated 2019-06-05

No results posted yet for this study

Summary

Following product approval, further confirmation of the MR Conditional Tachyarrhythmia Therapy Systems sensing and detection performance post MRI exposure will be obtained by actively monitoring de-identified device data obtained through the Medtronic CareLink® Network.

Conditions

  • Tachyarrhythmia

Interventions

DEVICE

Implant of an MR-conditional Tachy device system

Sponsors & Collaborators

Principal Investigators

  • Product Surveillance Registry Medtronic Product Surveillance Registry · Medtronic

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2018-12-31
Completion
2019-05-31

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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 NCT02849769 on ClinicalTrials.gov