Total Knee Replacement With Duracon® and Vanguard™ Prostheses

Stopped early

Conditions studied: Degenerative Arthritis, Osteoarthritis, Rheumatoid Arthritis, Knee Arthritis

In brief

The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.

Key facts

Study ID

NCT00588887

Run by

Biomet Orthopedics, LLC

People needed

150

Starts

2005-06-01

Expected to finish

2008-06-01

Last updated by the study team

2017-06-21

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.
• Patients requiring correction of varus, valgus, or posttraumatic deformity.
• Patients requiring correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

You may not qualify if…

• Patients with infection, sepsis, or osteomyelitis.

Where it is running

• Biomet Orthopedics, Inc. — Warsaw, Indiana, United States

Full record on ClinicalTrials.gov

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