Acute Pain Study Following Bunionectomy

Completed · Phase 2 · Has a placebo group

Conditions studied: Pain

In brief

The primary purpose of this study was to evaluate analgesic efficacy and safety of hydrocodone/acetaminophen extended release compared to placebo in the treatment of moderate to severe pain following bunionectomy.

Key facts

Study ID

NCT01333722

Run by

AbbVie (prior sponsor, Abbott)

People needed

100

Starts

2011-04-01

Expected to finish

2011-06-01

Last updated by the study team

2014-04-08

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who were in general good health, experiencing moderate to severe pain following bunionectomy

You may not qualify if…

• Subjects who underwent Base wedge osteotomy and / or Long-Z Hart bunionectomy procedures
• Drug allergies to hydrocodone, acetaminophen
• Clinically significant or uncontrolled medical disorders or illness - history of drug or alcohol abuse / addiction

Where it is running

• Site Reference ID/Investigator# 51464 — Pasadena, California, United States
• Site Reference ID/Investigator# 51602 — Austin, Texas, United States
• Site Reference ID/Investigator# 51344 — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.