N/A
Completed N=210
Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System
Osteoarthritis · Rheumatoid Arthritis · Post-traumatic Arthritis
Source: ClinicalTrials.gov NCT00487565 ↗
Enrolled (actual)
210
Serious AEs
13.3%
Results posted
Mar 2012
Primary outcomePrimary: Knee Active Flexion — 119.2 degrees
Summary
Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior stabilized design of the LCS® Complete Mobile-bearing Total Knee System
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Knee Active Flexion |
119.2 | — |
Eligibility Criteria
Inclusion Criteria
- 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
Exclusion Criteria
- 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.
Data sourced from ClinicalTrials.gov (NCT00487565). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.