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Methods for Effective Disposal of Surplus Analgesics to Facilitate Elimination

Not Applicable
Recruiting
Conditions
Surgery
Analgesics, Opioids
Interventions
Other: In-home drug disposal pouch
Other: Mail-in prepaid envelope
Registration Number
NCT05991687
Lead Sponsor
University of Michigan
Brief Summary

The primary objective is to evaluate the difference in outcomes for mail-in vs. in-home disposal methods for leftover prescription opioids after discharge from surgery.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Anticipated to be prescribed and use an opioid medication to treat acute pain after elective outpatient surgery
  • Opioid-naive
Exclusion Criteria
  • Inability to receive email and/or phone calls for follow up assessment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
In-homeIn-home drug disposal pouch-
Mail-inMail-in prepaid envelope-
Primary Outcome Measures
NameTimeMethod
Use of assigned disposal method2 weeks after surgery

Among patients who have leftover opioids, patient report of the use of their assigned mail-in or in-home method of disposal by 2 weeks after surgery.

Secondary Outcome Measures
NameTimeMethod
Use of any disposal method2 weeks after surgery

Patient-reported use of any method to dispose of leftover opioids, that includes assigned methods, safe methods, and other methods such as placing in the trash

Patient-Reported Satisfaction with Use of Disposal Method (study derived question)2 weeks after surgery

Patient report of overall satisfaction with use of the assigned disposal method, on a 0 (worst) to 10 (best) numeric scale

Feasibility of Intervention Measure (FIM)2 weeks after surgery
Use of safe disposal method2 weeks after surgery

Patient-reported use of a method for disposal of leftover opioids that includes mail-in, in-home, pharmacy drop off, or flushing down the toilet by

Acceptability of Intervention Measure (AIM)2 weeks after surgery

Trial Locations

Locations (1)

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

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