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Phase 3 N=89 Randomized Single-blind Health Services Research

Implantable Cardioverter-Defibrillator Use in the VA System

Cardiomyopathies

Enrolled (actual)
89
Serious AEs
5.6%
Results posted
Dec 2016
Primary outcome: Primary: Referral for Implantable Cardioverter Defibrillator — 11; 1 participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Clinical Reminder (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Stanford University
Primary completion
Jan 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Referral for Implantable Cardioverter Defibrillator
11; 1

Summary

Despite being a proven life-saving intervention in appropriately selected individuals, multiple studies continue to demonstrate low implantation of defibrillators in potential candidates. Based upon prior research, a major barrier to low utilization is low referral of potential candidates by healthcare providers. In this study, via brief clinical reminder placed in the electronic medical record, we ask healthcare providers who have not referred potential candidates for defibrillator the reasons for this decision and provide them with the tools for referral if appropriate.

Eligibility Criteria

Inclusion Criteria:Meeting published criteria for receipt of an implantable cardioverter defibrillator Exclusion Criteria:provider is not affiliated with the VA health care system
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01217827). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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