Study of Long-Acting Acetaminophen in Postoperative Dental Pain
Status:
Completed
Trial end date:
2014-04-01
Target enrollment:
Participant gender:
Summary
The purpose of the study is to evaluate the efficacy and safety of acetaminophen ER 1500 mg
(two 750 mg tablets) over 10 to 12 hours in the dental pain model following third molar
extraction(s) and to evaluate the pharmacokinetics of acetaminophen ER 1500 mg (two 750 mg
tablets) in a sub-group of subjects.
Phase:
Phase 2
Details
Lead Sponsor:
McNeil Consumer Healthcare Division of McNEIL-PPC, Inc.