About this trial
This study will evaluate if an intervention using academic detailing and audit and feedback impacts the specific pacemaker or implantable cardioverter-defibrillator (ICD) lead models implanted in Veterans.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Department of Veterans Affairs-based cardiac electrophysiologists who implant cardiovascular implantable electronic devices at three Veterans Integrated Service Networks (VISNs)
Disqualifiers
Not willing to participate in the study
Trial design
Single group
Treatments tested in this trial
Academic detailing and audit and feedback intervention
Other interventionAn academic detailing and audit and feedback intervention will be presented to VA cardiac electrophysiologists, and will include quantitative data about the individual physician's facilities cardiovascular implantable electronic device lead implants and national data on lead implants over the past year.
Treatment groups
Trial outcomes
Primary outcomes
Proportion of cardiovascular implantable electronic device leads that are of the lead model with the lowest failure rate
This outcome will be the proportion of cardiovascular implantable electronic device leads implanted in the 3 months post-intervention that are of the lead model with the lowest failure rate. The failure rates for the lead models will be available from VA data.
Sponsors and contacts
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VA Office of Research and Development
Lead sponsor
University of California, San Francisco
Collaborator
This trial is not recruiting at the moment. You can still explore other options: