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Clinical Trials/NCT04155229
NCT04155229
Completed
Not Applicable

Effect of Default Electronic Health Record Settings on Clinician Opioid Prescribing Patterns in Emergency Departments

University of California, San Francisco0 sites104 target enrollmentOctober 3, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Acute
Sponsor
University of California, San Francisco
Enrollment
104
Primary Endpoint
Dispense quantity of prescribed opioids
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The investigators conducted a prospective, block-randomized study to determine whether and to what extent changes in the default settings in the electronic medical record (EMR) affect opioid prescriptions for patients discharged from emergency departments (EDs).

Detailed Description

In two large, urban emergency departments, we randomly altered the pre-populated dispense quantities of discharge prescriptions for commonly-prescribed opioids over a series of five 4-week blocks. These changes were made without announcement, and providers were not informed of the study itself.

Registry
clinicaltrials.gov
Start Date
October 3, 2016
End Date
September 3, 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Discharge prescription from emergency for study drug: hydrocodone/acetaminophen, oxycodone, or oxycodone/acetaminophen.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Dispense quantity of prescribed opioids

Time Frame: Through study completion, approximately 340 days

The dispense quantity of prescribed study drugs was collected from the electronic medical record at each site. The mean and median quantities per prescription according to each study arm were compared.

Secondary Outcomes

  • Proportion ≤12(Through study completion, approximately 340 days)
  • Proportion at default setting(Through study completion, approximately 340 days)

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