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Clinical Trial Summary

Children presenting to the Emergency Room with the chief complaint of forearm injury and/or pain will be randomized to receive oral Oxycodone or Ibuprofen to control pain.


Clinical Trial Description

A randomized, blinded cohort study. Consented patients will be randomized to receive either ibuprofen or oxycodone after initial RN patient assessment in Emergency Department Triage determines a need for radiographs to evaluate for possible forearm fracture. Pain assessment scores will be determined at Triage and at 30-minute intervals throughout the patient's course until the patient is discharged home or additional analgesic medication is administered. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04523623
Study type Interventional
Source Washington University School of Medicine
Contact John E Graham
Phone 314-273-2734
Email grahamje@wustl.edu
Status Not yet recruiting
Phase N/A
Start date September 2020
Completion date February 2021

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