Skip to main content
Clinical Trials/NCT03030469
NCT03030469CompletedNot 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 enrollmentStarted: December 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10,000
Primary Endpoint
Initial prescription number of pills to dispense

Study 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).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Clinical Site 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

Arms & Interventions

10-pill default

Experimental

The intervention condition consists of a change to the electronic health record so that new opioid analgesic prescriptions automatically default to 10 pills (i.e., the "quantity dispensed" field is pre-populated). This value is modifiable by providers who can tailor the prescription based on clinical factors.

Intervention: Change in electronic health record default for new opioid analgesic prescriptions (Other)

5-pill default

Experimental

New opioid analgesic prescriptions will automatically default to 5 pills.

Intervention: Change in electronic health record default for new opioid analgesic prescriptions (Other)

Standard of care

No Intervention

The control condition will be the usual electronic health record interface. The default number of pills varies by medication, most medications currently have either a blank default or a default of 30 pills.

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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marcus Bachhuber

Assistant Professor

Montefiore Medical Center

Similar Trials