Advanced Bradycardia Device Feature Utilization and Clinical Outcomes II

NCT02577887 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2101

Last updated 2020-03-09

Study results available
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Summary

The purpose of this study is to characterize the utilization of diagnostics capabilities in St. Jude Medical pacemakers to manage patients with a standard bradycardia pacing indication.

Conditions

  • Standard Bradycardia Pacing Indication

Interventions

DEVICE

Patients implanted with a St. Jude Medical pacemakers

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Principal Investigators

  • Grant Kim · Abbott Medical Devices

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2017-11-25
Completion
2017-12-15

Countries

  • France
  • Germany
  • Italy
  • Japan

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 NCT02577887 on ClinicalTrials.gov