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Clinical Trial Summary

The purpose of this study is to evaluate two drug options for pain control in patients following wrist injury. Participants will be randomized to one of the 2 pain relief treatments to determine what treatment provides the most effective pain relief


Clinical Trial Description

The purposes of this noninferiority randomized clinical trial are to determine whether: 1. the most commonly used non-narcotic analgesic (ibuprofen 600 mg + acetaminophen 500 mg) provides pain relief that is not unacceptably worse than the most commonly prescribed narcotic (hydrocodone 5 mg + acetaminophen 500 mg) in patients with a hand or wrist fracture. 2. the following covariates affect pain outcomes: sex/gender, age, gender-related pain expectations, paid/unpaid work roles, comorbid health status, baseline pain intensity, and employment status. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03375593
Study type Interventional
Source Lawson Health Research Institute
Contact Joy C MacDermid, PhD
Phone 519-646-6100
Email jmacderm@uwo.ca
Status Recruiting
Phase Phase 4
Start date August 1, 2019
Completion date October 1, 2022

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