Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
DePuy Orthopaedics
Prospective, multi-center study to evaluate the clinical outcome of posterior stabilized design of LCS® Complete Mobile-Bearing Total Knee System. No comparison group. 12 month enrollment, 12 month post-operative evaluation. Follow-up intervals: Pre-op, 3 month, 6 month, and 12 month.
Age
18–80
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible 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 be 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.
Clareo Health | Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System
