Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04044820

Opioid Use Post-Discharge After Ambulatory Distal Arm Surgery

Led by University Health Network, Toronto · Updated on 2026-01-16

292

Participants Needed

1

Research Sites

408 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of this study is to determine if a standardized evidence-based opioid prescription following elective hand and forearm surgery at Toronto Western Hospital (TWH) will decrease the number of unused opioid pills consumed by patients while still maintaining adequate pain control as compared to usual treatment. Currently, no standardized prescription exists at our institution.

CONDITIONS

Official Title

Opioid Use Post-Discharge After Ambulatory Distal Arm Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting to Toronto Western Hospital for elective ambulatory hand and forearm surgery
Not Eligible

You will not qualify if you...

  • Chronic opioid treatment defined as more than 6 tablets of Oxycodone 5 mg (or equivalent) per day
  • Cognitive impairment or any condition causing inability to use 'as required' pain medication
  • Language barrier preventing completion of patient diary
  • Patient refusal to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Toronto Western Hospital

Toronto, Ontario, Canada, M5T2S8

Actively Recruiting

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Research Team

A

Anuj Bhatia, MD FRCPC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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