To Evaluate the Safety and Efficacy of Acetaminophen 650 mg and 1000mg in Dental Pain After Surgery

• Status: Completed
• Trial end date: 2011-01-01
• Target enrollment: 0
• Participant gender: All

Summary

The objective of this study is to evaluate the safety and efficacy of acetaminophen 650 mg and acetaminophen 1000 mg in dental surgery.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: McNeil Consumer Healthcare Division of McNEIL-PPC, Inc.
• Treatments: Acetaminophen

Criteria

Inclusion Criteria:

• Must be at least 16 and less than 51 years of age

• Must weigh at least 100 lbs with a body mass index of at least 18 and less than 30

• Must have up to four of their back teeth (third-molars) pulled

Exclusion Criteria:

• Cannot be allergic to acetaminophen (Tylenol)

• Cannot be pregnant (or planning to be pregnant) or nursing a baby

• Cannot have any other medical conditions that the investigator determines might compromise your safety or the study results