drugset / Trial / NCT02254525
A Multicenter Trial of the Efficacy and Safety of a New Formulation of Ibuprofen 800 mg Every 6 Hours in the Management of Postoperative Pain
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study is to study the efficacy of intravenous administration of ibuprofen compared to placebo in patients with postoperative pain and evaluate its tolerability and safety profile.
Timeline
- Start
- 2012-05
- Primary completion
- 2014-06
- Completion
- 2014-07
Outcome
Outcome not reported
Stopped: “Sample not reached in traumathology arm”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ibuprofen | Small molecule | 800 mg | Intravenous |
Indications
No indication recorded.