Default Dosing Settings for Opioid Prescriptions to Adolescents and Young Adults After Tonsillectomy
Completed · Not applicable
Conditions studied: Tonsillectomy
In brief
This study will evaluate whether lowering the default number of doses for opioid prescriptions written in an electronic health record system can decrease opioid prescribing without causing unintended consequences such as worsened pain control.
Key facts
- Study ID
- NCT04066829
- Run by
- University of Michigan
- People needed
- 198
- Starts
- 2019-10-01
- Expected to finish
- 2021-07-31
- Last updated by the study team
- 2022-11-01
Who can join
Age: 12 and older, up to 25. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adolescents and young adults aged 12-25 years undergoing tonsillectomy at C.S. Mott Hospital, University Hospital, Brighton Center for Specialty Care, or Livonia Center for Specialty Care from October 2019-July 2021, excluding April-May 2020 (owing to suspension of elective procedures due to COVID-19).
- Surgeon belongs to the Department of Otolaryngology at the University of Michigan Medical School
- Patients are not any of the following: patients living in foster care or with a legal guardian, patients with medical complexity or developmental delays, non-English speaking patients, patients with recent suicidal ideation documented in their chart, or patients undergoing emergent tonsillectomy.
You may not qualify if…
- Patients with prescription opioid use prior to surgery
- Patients undergoing additional procedures at the same time as tonsillectomy (other than minor procedures such as tympanostomy tube placement)
- Patients enrolled in another study
- Patients who are not prescribed opioids post-operatively at discharge
- Patients who are enrolled in the Michigan Pain-control Optimization Pathway (M-POP), which includes education about pain management and a small initial opioid prescription
- Patients with hospitalization with length of stay > 1 day after surgery
- Patients who decline to enroll
- Additional exclusion criteria for secondary analysis: Patients who do not complete the baseline and post-operative day 14 surveys
Where it is running
- The University of Michigan — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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