Clinical Trials Directory

Trials / Completed

CompletedNCT01686802

Post-operative Oral Morphine Versus Ibuprofen

Oral Morphine Versus Ibuprofen for Post-operative Pain Management in Children: a Randomized Controlled Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
132 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
All
Age
5 Years – 17 Years
Healthy volunteers
Accepted

Summary

Children 5-17 years of age who have undergo orthopedic day surgical procedures for definitive management of fractures, tendon release, etc. will be randomized to receive either ibuprofen or oral morphine as needed for pain relief for 48 hours post-operatively at home. Pain will be assessed using the self-report Faces pain scale revised (FPS-R). We hypothesize that oral morphine will result in significantly lower pain scores on the Faces Pain Scale Revised (FPS-R) compared to ibuprofen. It is hoped that the results of this trial will create a new option for post-operative pain management in children.

Conditions

Interventions

TypeNameDescription
DRUGoral morphine
DRUGIbuprofen

Timeline

Start date
2012-09-01
Primary completion
2016-09-01
Completion
2016-09-01
First posted
2012-09-18
Last updated
2016-12-28

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01686802. Inclusion in this directory is not an endorsement.