Patient Profiling and Provider Feedback to Reduce Adverse Drug Events

Completed · Not applicable

Conditions studied: Adverse Drug Events

In brief

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.

Key facts

Study ID

NCT00013143

Run by

US Department of Veterans Affairs

People needed

1200

Starts

2001-06-01

Expected to finish

2003-01-01

Last updated by the study team

2015-04-07

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• patient must be alive
• patient must be currently active in GLA system
• medication for which alert was generated must be currently active
• patient provider must not be Peter Glassman

Where it is running

• VA Greater Los Angeles Healthcare System, West Los Angeles, CA — West Los Angeles, California, United States

Full record on ClinicalTrials.gov

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