N/A
N=595
Implementation of Real-time ADE Surveillance and Decision Support
Adverse Drug Events
Bottom Line
View on ClinicalTrials.gov: NCT00780572 ↗Enrolled (actual)
595
Serious AEs
0.0%
Results posted
Nov 2015
Primary outcome: Primary: Time to Intervention Once an ADE Alert Has Fired in CPRS — 6.8; 8 hours to intervention — p=0.6680
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- ADE alert assistant (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- VA Office of Research and Development
- Primary completion
- Sep 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Intervention Once an ADE Alert Has Fired in CPRS |
6.8; 8 | 0.6680 |
Summary
The purpose of this study is to determine if an electronic alerting technology improves time to intervention for possible ADEs, identify what factors affect adoption of ADE alerts, and whether there is a cost benefit associated with the alerting technology.
Eligibility Criteria
Inclusion Criteria
- All patients admitted to the SLCVAMC at time of study.
Exclusion Criteria
- There are no exclusions.
Data sourced from ClinicalTrials.gov (NCT00780572). 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.