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Electronic Defaults to Reduce Opioid Prescribing in Emergency Department and Primary Care Settings

A Cluster-randomized Trial of Modifying Electronic Health Record Defaults to Reduce the Prescribed Quantity of Opioid Analgesics in Primary Care and Emergency Department Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03003832
Enrollment
15000
Registered
2016-12-28
Start date
2016-12-31
Completion date
2018-07-13
Last updated
2018-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain

Brief summary

The goal of this research is to investigate the impact of changing opioid analgesic prescribing defaults on the quantity of opioids prescribed for acute non-cancer pain in adult primary care and emergency department settings. We will change prescribing defaults for select short-acting opioid analgesics including immediate release oxycodone and hydrocodone as well as codeine and tramadol, including their co-formulations with acetaminophen. In a cluster-randomized trial of matched pairs of Montefiore Medical Center clinical sites, stratified by specialty and teaching status, we will evaluate the impact of this intervention on patient-level outcomes using 18 months of data (6 months pre-intervention and 12 months post-intervention).

Interventions

Sponsors

Albert Einstein College of Medicine
CollaboratorOTHER
Montefiore Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Clinical Site Inclusion Criteria: * Primary care clinic (internal medicine, family medicine, or urgent care) or emergency department within Montefiore Medical Center Patient Inclusion Criteria: * Received a new opioid analgesic prescription, defined as no opioid analgesic prescription in the preceding 6 months Patient

Exclusion criteria

* Cancer diagnosis code within the past 1 year

Design outcomes

Primary

MeasureTime frameDescription
Initial prescription <= 10 pills (y/n)Through study completion (18 months)Extracted from the electronic medical record

Secondary

MeasureTime frameDescription
Initial prescription morphine milligram equivalentsThrough study completion (18 months)Extracted from the electronic medical record
Opioid analgesic re-order (y/n)Within 30 days after the initial prescriptionExtracted from the electronic medical record
Total opioid analgesic pills prescribed, including re-ordersWithin 30 days after the initial prescriptionExtracted from the electronic medical record
Initial prescription number of pillsThrough study completion (18 months)Extracted from the electronic medical record
Outpatient visitsWithin 30 days after the initial prescriptionExtracted from the electronic medical record
Emergency department visitsWithin 30 days after the initial prescriptionExtracted from the electronic medical record
HospitalizationsWithin 30 days after the initial prescriptionExtracted from the electronic medical record
Total morphine milligram equivalents prescribed, including re-ordersWithin 30 days after the initial prescriptionExtracted from the electronic medical record

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026