drugset / Trial / NCT00346268

Morphine-Sparing Efficacy Of Parecoxib In Pain Treatment After Radical Prostatectomy

NCT00346268

Phase 4 Terminated 105 enrolled Pfizer
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to demonstrate the opioid-sparing efficacy of parecoxib 40 mg intravenously given as a loading dose followed by 20 mg intravenously in the 24 hours after the end of surgery.

Timeline

Start
2006-12
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Parecoxib Small molecule 20 mg Intravenous
Comparator Morphine Other / unclassified 1 mg

Indications

No indication recorded.