Agility LP Ankle Arthroplasty Outcomes

Completed

Conditions studied: Rheumatoid Arthritis of Ankle, Osteoarthritis of Ankle, Traumatic Arthritis of Ankle

In brief

This is a research study which is being done to determine the outcomes following Agility LP ankle replacement. This implant was approved by the FDA in 2007 and has been used since then with good early results. You are being asked to volunteer for this study because you have undergone Total Ankle Arthroplasty with Agility LP prosthesis. The purpose of the study is to compare the range of motion, level of pain and function during daily living prior to and after your ankle surgery.

Key facts

Study ID

NCT01366872

Run by

Orthopaedic Associates of Michigan, PC

People needed

50

Starts

2010-12-01

Expected to finish

2012-09-01

Last updated by the study team

2012-12-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Over 18 years old
• Can comprehend and sign the informed consent
• Patient must have undergone Agility LP ankle replacement between January 2006 to June 2008

You may not qualify if…

• Patient has had following procedures on the study limb within two years of TAA
• Revision of TAA
• Ankle arthrodesis
• Amputation
• Agility LP arthroplasty was done as a revision procedure for a failed TAA or as a takedown of ankle fusion.
• Any condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.

Where it is running

• Orthopaedic Associates of Michigan, PC — Grand Rapids, Michigan, United States

Full record on ClinicalTrials.gov

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