drugset / Trial / NCT00293631

Study of Lornoxicam or Ketorolac or Placebo for Post-Operative Pain After Bunionectomy

NCT00293631

Phase 2 Completed 100 enrolled POZEN
RandomizedParallel-groupDouble-blindTreatment

Summary

To determine whether a single dose of intravenous lornoxicam is superior to intravenous placebo for management of post-operative pain in patients who have surgical removal of a bunion on the lower extremity. One-fourth of patients in this study will receive a single dose of intravenous ketorolac for management of pain and one-fourth of patients in this study will receive a single dose of an intravenous placebo.

Timeline

Start
2005-11
Primary completion
2006-03
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketorolac Other / unclassified 30 mg Intravenous
Subject Lornoxicam Small molecule 8 mg Intravenous
Subject Lornoxicam Small molecule 16 mg Intravenous

Indications

No indication recorded.