Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System

Completed · Not applicable

Conditions studied: Osteoarthritis, Rheumatoid Arthritis, Post-traumatic Arthritis, Juvenile Arthritis

In brief

Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior stabilized design of the LCS® Complete Mobile-bearing Total Knee System

Key facts

Study ID

NCT00487565

Run by

DePuy Orthopaedics

People needed

210

Starts

2006-09-01

Expected to finish

2011-02-01

Last updated by the study team

2013-08-14

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• M/F
• 18-80
• Diagnosis of osteoarthritis, rheumatoid , post-traumatic, inflammatory, juvenile arthritis.
• Skeletally mature, sufficient bone stock to seat and support prosthesis
• Willing/able return for follow-up.
• Subject is willing and able to provide informed patient consent for participation in the study

You may not qualify if…

• History of recent/active joint sepsis, charcot neuropathy, psycho-social disorders, prior knee arthroplasty on affected site, metabolic disorders of calcified tissue
• Communicable diseases that may limit follow-up
• Medical-legal or workers compensation claims.

Where it is running

• Colorado Joint Replacement — Denver, Colorado, United States
• Joint Reconstruction Center — Pittsburgh, Pennsylvania, United States
• Jordan-Young Institute — Virginia Beach, Virginia, United States

Full record on ClinicalTrials.gov

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