The purpose of this project is to compare the analgesic efficacy and safety of a single dose of etodolac SR (1200 mg or 400 mg) to two doses of conventional etodolac (400 mg q 8hr, or 200 mg q 8hr) and placebo in patients following the removal of impacted wisdom teeth. a secondary objective is to evaluate the relationship between etodolac plasma levels and analgesia.

Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
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