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Clinical Trials/NCT04044105
NCT04044105
Completed
Not Applicable

Impacting the Disposal of Unused Opioid Analgesics Through Education in the Orthopaedic Population: A Randomized Control Trial

Rush University Medical Center1 site in 1 country563 target enrollmentAugust 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Opioid Use and Disposal
Sponsor
Rush University Medical Center
Enrollment
563
Locations
1
Primary Endpoint
Disposal rates
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to compare the rates of proper opioid disposal in patients receiving an educational brochure compared to an automated text message delivered directly to patients' cell phones alongside the brochure, compared to no education on the subject.

Detailed Description

Opioids are used to treat acute pain after surgery, but can lead to misuse and abuse. Very few patients properly dispose of unused opioids and the majority of opioids are stored in the home in unlocked containers as opposed to being properly disposed of. Improper disposal of opioid medications is a concern due to the potential for nonmedical use and has the potential to cause injury or death for patients and their family members that can access the medications. The purpose of this study is to compare the rates of proper opioid disposal in patients receiving an educational brochure compared to an automated text message delivered directly to patients' cell phones alongside the brochure, compared to no education on the subject. There is evidence that an educational brochure significantly increases proper disposal rates, albeit only to about 25%. The goal of this study is to evaluate the impact of an educational pamphlet on proper opioid disposal in the total joint arthoplasty population, and to see if the addition of a text messaging system can increase further increase proper disposal rates.

Registry
clinicaltrials.gov
Start Date
August 1, 2018
End Date
December 31, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Craig J Della Valle, MD

Professor of Orthopaedic Surgery

Rush University Medical Center

Eligibility Criteria

Inclusion Criteria

  • Any patient undergoing primary total hip or knee arthroplasty
  • Age ≥18 years old

Exclusion Criteria

  • Patients allergic to oxycodone
  • Patients consuming opioids during the 4 weeks prior to surgery
  • Patients with a history of opioid dependence
  • Patients undergoing revision total knee or hip arthroplasty
  • Non-English speaking patients
  • Age \<18 years old

Outcomes

Primary Outcomes

Disposal rates

Time Frame: 6 weeks after surgery

The rate of an arm's disposal is calculated by comparing the number that properly disposed of their excess medication to the number that did not

Secondary Outcomes

  • Continued taking opiate rate(6 weeks after surgery)

Study Sites (1)

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