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Completed
NCT06271668
Clinical Decision Support to Improve System Naloxone Co-prescribing
Conditions: Medication Abuse, Harm Reduction, Opioid Overdose, Opioid Prescribing
Sex: All
Ages: 12 Years – 89 Years
Healthy volunteers: Yes
Enrollment: 114272
Sponsor: University of Colorado, Denver
Location: University of Colorado Hospital Aurora Colorado
Summary
The objective of this study is to evaluate the impact of a clinical decision support (CDS) alert to facilitate the co-prescribing of naloxone, an opioid overdose reversal agent, with high-risk opioid prescriptions. Prescribing naloxone with opioids is a best practice described in the 2022 US Center for Disease Control and Prevention (CDC) guidelines on opioid prescribing. The CDS can improve quality of care delivered by improving compliance with the guideline defined best practices. The project will compare CDS alert facilitated co-prescribing of naloxone with high-risk opioid prescriptions vs usual care to evaluate the effectiveness of the CDS alert for improving naloxone prescribing. The patients are not assigned to an intervention and will be receiving any changes in care as part of their routine medical care, rather than a specific intervention that is distinct from their usual medical care. The researchers hypothesize that the CDS alert will be acceptable to providers while increasing naloxone co-prescribing which will reduce the number of opioid overdoses in subsequent 6 months.
Eligibility Criteria
Inclusion Criteria:
* Patients receiving an opioid prescription at discharge from inpatient/ED or close visit in outpatient settings where the clinical decision support (CDS) is implemented
Exclusion Criteria:
* Patients \89 year of age
* Cancer diagnosis
* Hospice care/palliative care
* Sickle cell disease diagnosis
* Patients who arrived in error
* Patients who were triaged to obstetrics
Source: ClinicalTrials.gov (NCT06271668). StuddyBuddy aggregates publicly available trial information.