At a glance
ClinicalIndex Comparison RecordN/ACompleted· 595 enrolled
Drug / intervention
ADE alert assistantbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Implementation of Real-Time ADE Surveillance and Decision Support
In Brief
A clinical study evaluating ADE alert assistant for Adverse Drug Events. Completed, enrolled 595 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdverse Drug Events
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 2008
Enrollment StartDec 2008
Primary CompletionSep 2010
Study CompletionMar 2011
TodayJul 2026
First PostedOct 27, 2008
Enrollment StartDec 1, 2008
Primary CompletionSep 1, 2010
Study CompletionMar 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 17.7 years ago
Interventions
ADE alert assistantbehavioral
A note in CPRS alerting providers that patients are at risk for an adverse event based on prescription and lab value histories.