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A Randomized, Parallel-Group, Double-Blind, Single-Dose Study Evaluating the Efficacy and Safety of Intravenous Lornoxicam (8 mg and 16 mg) Compared to Intravenous Placebo and Ketorolac 30 mg in Management of Acute Postoperative Pain Following Orthopedic Surgery (Bunionectomy).
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.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Advanced Clinical Research Institute
Anaheim, California, United States
Start Date
November 1, 2005
Primary Completion Date
March 1, 2006
Completion Date
March 1, 2006
Last Updated
December 3, 2012
100
Estimated participants
Lornoxicam 8 mg
DRUG
Lornoxicam 16 mg
DRUG
Ketorolac 30 mg
DRUG
Placebo
DRUG
Lead Sponsor
POZEN
Data Source & Attribution
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