900
Participants
Start Date
September 30, 2010
Primary Completion Date
December 31, 2011
Study Completion Date
June 30, 2012
Parecoxib
The study group will receive first dose of intravenous (IV) injection of parecoxib sodium 40 mg (in a volume of 2 ml) 60 min before the anticipated end of surgery, followed 2 ml IV injection of parecoxib 40 mg will be occurred at 12, 24 and 36 h after the first dose of parecoxib.
RECRUITING
The First Affiliated Hospital of Sun Yat-sen University, Guangzhou
Collaborators (1)
Pfizer
INDUSTRY
First Affiliated Hospital, Sun Yat-Sen University
OTHER