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Imaging Study of Lead Implant for His Bundle Pacing

NCT03294317 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2021-06-01

Study results available
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Summary

The purpose of this research study is to assess the implant success proportion of the Medtronic SelectSecure MRI SureScan Model 3830 pacing lead at the bundle of His for His bundle pacing.

Conditions

  • Cardiac Pacemaker, Artificial

Interventions

DEVICE

His bundle pacing

Medtronic SelectSecure SureScan MRI model 3830 lead

Sponsors & Collaborators

  • Medtronic Cardiac Rhythm and Heart Failure

    lead INDUSTRY

Principal Investigators

  • Pugazhendhi Vijayaraman, MD · Geisinger Wyoming Valley Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-29
Primary Completion
2019-04-24
Completion
2020-01-24
FDA Device
Yes

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 NCT03294317 on ClinicalTrials.gov