At a glance
ClinicalIndex Comparison RecordN/ACompleted· 1,200 target
Drug / intervention
Patient risk profiling (potential ADEs) w/provider feedbackbehavioral
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.
Patient Profiling and Provider Feedback to Reduce Adverse Drug Events
In Brief
A clinical study evaluating Patient risk profiling (potential ADEs) w/provider feedback for Adverse Drug Events. Completed, enrolled 1,200 participants across 1 site.
Detailed Summary
Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAdverse Drug Events
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 2001
Enrollment StartJun 2001
Study CompletionJan 2003
TodayJul 2026
First PostedMar 16, 2001
Enrollment StartJun 1, 2001
Study CompletionJan 1, 2003
TodayJul 2, 2026
Posted 25.3 years ago
Interventions
Patient risk profiling (potential ADEs) w/provider feedbackbehavioral