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
| Type | Name | Description |
|---|---|---|
| DRUG | oral morphine | |
| DRUG | Ibuprofen |
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.