ProMRI ICD/CRT-D Post Approval Study

NCT02933619 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24249

Last updated 2019-10-22

No results posted yet for this study

Summary

Following product approval, confirmation of appropriate VF episode detection after MRI exposure of the ProMRI ICD/CRT-D systems and to evaluate left ventricular pacing threshold changes post-MRI.

Conditions

  • Tachyarrhythmia

Sponsors & Collaborators

  • Biotronik, Inc.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2019-04-30
Completion
2019-04-30

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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 NCT02933619 on ClinicalTrials.gov