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OpenTrials
Completed

NCT Number: NCT01091038

Improving Safety by Basic Computerizing Outpatient Prescribing

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

Completed

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Wishard Helath Services, Indianapolis, Indiana, United States

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Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Basic Clinical Decision Support

Other

The computerized physician order entry (CPOE) intervention provides physicians with a menu of medications from the formulary, default doses, and a range of potential doses for each medication. Physicians were required to enter dosage, route, and frequency for all orders. Also, CPOE ensured that all orders were legible and included the prescribing physician's signature. For a number of medications, the system displayed relevant laboratory results on the screen at the time of ordering. Other features included consequent orders, which are orders that should follow from other orders, and drug-allergy checking, drug-drug interaction checking, and drug-laboratory checking. This included checking for the most frequent drug allergies, about 80 carefully selected drug-drug interactions, and several drug-laboratory combinations

Routine care

Other

Routine Care

Primary outcomes

  1. Adverse Drug Events

    Time frame: 6 months

    Adverse drug events are measured through use of a computerized surveillance system augmented by focused structured human review

  2. Medical Errors

    Time frame: 6 months

    Medical Errors are identified through a computerized surveillance system with structured human review

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Collaborators

  • Brigham and Women's Hospital

Registry information

Important dates

Study start
2001
Primary completion
2007
Study completion
2007
First posted
Mar 23, 2010
Registry last updated
Oct 12, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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