Clinical Trials Directory

Trials / Completed

CompletedNCT00235027

Improving Safety By Computerizing Outpatient Prescribing

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
701 (actual)
Sponsor
Agency for Healthcare Research and Quality (AHRQ) · Federal
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Patient safety is at the forefront of critical issues in health care. Medications are the single most frequent cause of adverse events, and in the inpatient setting adverse drug events (ADEs) are common, expensive, injurious to patients, and often preventable. Relatively little, however, is known about the frequency of ADEs in the ambulatory setting, how to monitor for outpatient ADEs, or on the impact of prevention strategies such as computerization of prescribing supplemented by decision-support.

Detailed description

Specific Aim 1: Increase routine identification of outpatient adverse drug events (ADEs) through development of a computerized ADE detection monitor. Specific Aim 2: Use basic computerized outpatient prescribing to reduce preventable ADEs in a diverse array of outpatient settings. Specific Aim 3: Use advanced decision-support within computerized prescribing to reduce the frequency of preventable ADEs, medication errors, and potential ADEs.

Conditions

Interventions

TypeNameDescription
OTHERAdverse Drug Event MonitoringThe intervention in this study is the presentation of medication safety alerts in the electronic medical record to improve patient outcomes and safety.

Timeline

Start date
2000-08-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2005-10-10
Last updated
2015-07-21

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00235027. Inclusion in this directory is not an endorsement.