NCT00013143View on ClinicalTrials.gov

Patient Profiling and Provider Feedback to Reduce Adverse Drug Events

NACompletedINTERVENTIONAL
Enrollment

1,200

Participants

Timeline

Start Date

June 30, 2001

Study Completion Date

January 31, 2003

Conditions
Adverse Drug Events
Interventions
BEHAVIORAL

Patient risk profiling (potential ADEs) w/provider feedback

Trial Locations (1)

90073

VA Greater Los Angeles Healthcare System, West Los Angeles, CA, West Los Angeles

All Listed Sponsors
lead

US Department of Veterans Affairs

FED

NCT00013143 - Patient Profiling and Provider Feedback to Reduce Adverse Drug Events | Biotech Hunter | Biotech Hunter