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

Completed · Phase 3 · Has a placebo group

Conditions studied: Pain

In brief

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

Key facts

Study ID

NCT01115673

Run by

McNeil Consumer Healthcare Division of McNEIL-PPC, Inc.

People needed

540

Starts

2010-06-01

Expected to finish

2011-01-01

Last updated by the study team

2012-05-28

Who can join

Age: 16 and older, up to 50. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Jean Brown Research — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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