91
Participants
Start Date
April 30, 2003
Study Completion Date
March 31, 2004
Parecoxib/Valdecoxib
A single 40mg dose of intravenous (IV) parecoxib sodium administered on Day 1 immediately before the surgical procedure as part of the Investigator's usual analgesic management practice, followed by oral doses of valdecoxib 40 mg (2 x 20 mg tablets) at 6-8 hours post-surgery on Day 1 and in the morning of Day 2 and Day 3
Placebo
A single dose of IV saline (placebo) administered on Day 1 immediately before the surgical procedure as part of the Investigator's usual analgesic management practice, followed by oral doses of placebo (2 x matching valdecoxib 20 mg tablets) at 6-8 hours post-surgery on Day 1 and in the morning of Day 2 and Day 3
Pfizer Investigational Site, Randwick
Pfizer Investigational Site, Westmead
Pfizer Investigational Site, Heidelberg
Pfizer Investigational Site, Prahran
Pfizer Investigational Site, Coopers Plain
Pfizer Investigational Site, Townsville
Pfizer Investigational Site, Perth
Pfizer Investigational Site, Port Macquarie
Lead Sponsor
Pfizer
INDUSTRY