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
| Type | Name | Description |
|---|---|---|
| OTHER | Default 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.