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Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programming

NCT00856349 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4384

Last updated 2014-07-03

Study results available
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Summary

The purpose of this clinical trial is to determine whether periodic therapy programming reports illustrating physician usage of shock reduction programming can increase utilization of recommended programming guidelines for defibrillators.

Conditions

Interventions

BEHAVIORAL

Therapy Programming Report (TPR)

Center-specific therapy programming reports (TPRs) illustrating physician usage of shock reduction programming are provided to each center approximately 9-12 months after their first enrollment and monthly thereafter throughout the study.

Sponsors & Collaborators

  • Medtronic Cardiac Rhythm and Heart Failure

    lead INDUSTRY

Principal Investigators

  • Marc Silver, M.D. · Raleigh Cardiology Associates

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2013-03-31
Completion
2013-03-31

Countries

  • United States
  • Argentina
  • Australia
  • Canada
  • China
  • Hong Kong
  • India
  • Mexico
  • New Zealand
  • Singapore
  • South Korea
  • Taiwan

Study Locations

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Entities

Diseases

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 NCT00856349 on ClinicalTrials.gov