CompletedPhase 2/3

Improving Safety by Basic Computerizing Outpatient Prescribing

United States228 participantsStarted 2001-08

Plain-language summary

The study will measure the effect of basic clinical decision support on medical errors and adverse drug events in the ambulatory setting.

Who can participate

SexALL

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Inclusion Criteria: * provider practicing at sites implementing order entry with basic clinical decision support using either the longitudinal medical record (LMR) or Medical Gopher Exclusion Criteria: * provider or practice unwilling to participate

What they're measuring

Adverse Drug Events

Timeframe: 6 months

Medical Errors

Timeframe: 6 months

Trial details

NCT IDNCT01091038

SponsorIndiana University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2007-08

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