Last reviewed · How we verify
A Multicentre, Double-Blind, Placebo-Controlled Study of the Recovery Benefits Following Treatment With a Cox-2 Regimen in Patients Undergoing Elective Laparoscopic Intra-Peritoneal Abdominal Surgery
The purpose of this study is to evaluate morphine intake in the first 4 hours after abdominal surgery. Morphine intake is compared between patients on placebo and patients on parecoxib/valdecoxib.
Details
| Lead sponsor | Pfizer |
|---|---|
| Phase | Phase 3 |
| Status | TERMINATED |
| Enrolment | 91 |
| Start date | 2003-04 |
| Completion | 2004-03 |
Conditions
- Pain
Interventions
- Parecoxib/Valdecoxib
- Placebo
Primary outcomes
- Total intake of morphine in first 4 hours post-surgery upon waking of patients receiving parecoxib versus control group. — 4 hours
Countries
Australia