Implementation of Real-time ADE Surveillance and Decision Support
Completed · Not applicable
Conditions studied: Adverse Drug Events
In brief
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.
Key facts
- Study ID
- NCT00780572
- Run by
- VA Office of Research and Development
- People needed
- 595
- Starts
- 2008-12-01
- Expected to finish
- 2011-03-01
- Last updated by the study team
- 2015-12-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients admitted to the SLCVAMC at time of study.
You may not qualify if…
- There are no exclusions.
Where it is running
- VA Health Care Salt Lake City — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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