drugset / Trial / NCT01859585

Efficacy Parecoxib and Ketorolac as Preemptive Analgesia in Spine Fusion

NCT01859585

Phase 4 Completed 96 enrolled Prince of Songkla University
RandomizedParallel-groupTriple-blindSupportive care

Summary

The purpose of this study is to evaluate the efficacy of Parecoxib and Ketorolac as a preemptive analgesia in patients undergoing lumbar spinal fusion.

Timeline

Start
2011-03
Primary completion
2013-01
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketorolac Other / unclassified 30 mg Intravenous
Subject Parecoxib Small molecule 40 mg Intravenous

Indications

No indication recorded.