NCT Number: NCT03030469
Electronic Defaults to Reduce Opioid Prescribing in Dentistry Practices
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).
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
- None
Treatment and study plan
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
Time frame: Through study completion (18 months)
From the electronic health record
-
Opioid analgesic reorder (y/n)
Time frame: Within 30 days after the initial prescription
From the electronic health record
-
Total opioid analgesic pills to dispense, including re-orders
Time frame: Within 30 days after the initial prescription
From the electronic health record
-
Total morphine milligram equivalents to dispense, including re-orders
Time frame: Within 30 days after the initial prescription
From the electronic health record
-
Outpatient visits
Time frame: Within 30 days after the index prescription
From the electronic health record
-
Emergency department visits
Time frame: Within 30 days after the initial prescription
From the electronic health record
-
Hospitalizations
Time frame: Within 30 days after the initial prescription
From the electronic health record
Interested in participating?
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Notify MeSponsors and collaborators
Lead sponsor
Montefiore Medical Center
Other
Collaborators
- Albert Einstein College of Medicine
Registry information
Official study title
A Cluster-randomized Trial of Modifying Electronic Health Record Defaults to Reduce the Prescribed Quantity of Opioid Analgesics in Dentistry Practices
Important dates
- Study start
- 2016
- Primary completion
- 2018
- Study completion
- 2018
- First posted
- Jan 25, 2017
- Registry last updated
- Aug 14, 2018
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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