Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction

Completed · Phase 2 · Has a placebo group

Conditions studied: Pain

In brief

The purpose of this study was to evaluate analgesic efficacy and safety of hydrocodone/acetaminophen compared to placebo in moderate to severe pain following molar extraction.

Key facts

Study ID

NCT00935311

Run by

AbbVie (prior sponsor, Abbott)

People needed

122

Starts

2009-06-01

Expected to finish

2009-08-01

Last updated by the study team

2014-04-08

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who are in general good health, experiencing moderate to severe pain after surgical extraction of 2 or more third molars and who are willing to remain confined until the morning after surgery for study procedures

You may not qualify if…

• Allergies to study medications
• History of multiple drug allergies
• Unable to stop excluded medications
• Clinically significant laboratory abnormalities at Screening
• Significant medical condition at Screening
• Women who are pregnant or breast feeding

Where it is running

• Site Reference ID/Investigator# 20745 — Austin, Texas, United States
• Site Reference ID/Investigator# 20743 — San Marcos, Texas, United States
• Site Reference ID/Investigator# 20744 — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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