View Clinical Trial (Medical Research Study)
Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System - NCT00487565-23462(Clinical Trial 172745)
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Virginia Beach |
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State:
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VA |
| Zip Code: |
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23462 |
| Conditions: |
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Osteoarthritis - Rheumatoid Arthritis - Post-Traumatic Arthritis - Juvenile Arthritis |
| Purpose: |
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Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior
stabilized design of the LCS® Complete Mobile-bearing Total Knee System
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| Study summary: |
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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. |
| Criteria: |
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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.
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. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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October 7, 2010 |
Modifications to
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