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Clinical Trials/NCT03030469
NCT03030469
Completed
Not Applicable

A Cluster-randomized Trial of Modifying Electronic Health Record Defaults to Reduce the Prescribed Quantity of Opioid Analgesics in Dentistry Practices

Montefiore Medical Center0 sites10,000 target enrollmentDecember 2016
ConditionsAcute Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Pain
Sponsor
Montefiore Medical Center
Enrollment
10000
Primary Endpoint
Initial prescription number of pills to dispense
Status
Completed
Last Updated
7 years ago

Overview

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 dentistry 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 three Montefiore Medical Center dentistry sites, 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).

Registry
clinicaltrials.gov
Start Date
December 2016
End Date
July 13, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marcus Bachhuber

Assistant Professor

Montefiore Medical Center

Eligibility Criteria

Inclusion Criteria

  • Dentistry clinic within Montefiore Medical Center
  • Patient Inclusion Criteria:
  • Received a new opioid analgesic prescription, defined as no opioid analgesic prescription in the preceding 6 months

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Initial prescription number of pills to dispense

Time Frame: Through study completion (18 months)

From the electronic health record

Secondary Outcomes

  • Initial prescription morphine milligram equivalents to dispense(Through study completion (18 months))
  • Hospitalizations(Within 30 days after the initial prescription)
  • Opioid analgesic reorder (y/n)(Within 30 days after the initial prescription)
  • Total opioid analgesic pills to dispense, including re-orders(Within 30 days after the initial prescription)
  • Outpatient visits(Within 30 days after the index prescription)
  • Total morphine milligram equivalents to dispense, including re-orders(Within 30 days after the initial prescription)
  • Emergency department visits(Within 30 days after the initial prescription)

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