Clinical Trials Directory

Trials / Completed

CompletedNCT04155229

EMR Defaults to Nudge Opioid Prescribing

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
104 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERDefault settings for opioid prescriptions (acetaminophen/hydrocodone, oxycodone, acetaminophen/oxycodone)For each of the arms, the investigators modified the default setting for the dispense quantity of study opioids on the electronic medical record settings for discharge prescriptions. Study drugs include acetaminophen 325mg + hydrocodone 5mg, acetaminophen 325mg + hydrocodone 7.5mg, acetaminophen 325mg + hydrocodone 10mg, oxycodone 5mg, acetaminophen 325mg + oxycodone 5mg, acetaminophen 325mg + oxycodone 10mg.

Timeline

Start date
2016-10-03
Primary completion
2017-09-03
Completion
2017-09-03
First posted
2019-11-07
Last updated
2019-11-07

Source: ClinicalTrials.gov record NCT04155229. Inclusion in this directory is not an endorsement.