drugset / Trial / NCT01082471
An Efficacy and Safety Study to Compare Morphine 6-glucuronide (M6G) and Morphine in Patients Suffering With Post-Operative Pain for at Least 24 Hours
RandomizedParallel-groupQuadruple-blindTreatment
Summary
To compare the incidence and severity of nausea in the study treatment groups, during the 18-hour period starting 6 hours after titration to pain relief; following confirmation of the assumption of non-inferiority between the two groups of pain relief over the 24 hour post-operative period. Pain relief and nausea will be determined by measuring the areas under the curves of pain intensity and nausea verbal rating scale scores.
Timeline
- Start
- 2005-11
- Primary completion
- 2006-11
- Completion
- 2006-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MORPHINE GLUCURONIDE | Small molecule | — | — |
| Comparator | Morphine | Other / unclassified | — | — |
Indications
No indication recorded.