This study is a retrospective, multi-center study, with one single remote follow up contact. This study will include a minimum of 80 patients and a maximum 100 patients who have been treated with the ConforMIS iTotal PS knee product.
Patients will be contacted either by phone or email for a single remote follow-up. Retrospective data will be collected from medical records including pre-operative, operative and any follow up visits which have occurred since implantation as available. . All data will be collected from existing medical records and from single follow up call/email. * Demographics and Medical History * Pre \& Post-Operative Data including Range of Motion * Surgical Data * Survivorship (phone/email or last known visit) * Patient Reported Outcomes (phone/email single time point visit) * Patient Satisfaction * KOOS Jr.
Study Type
OBSERVATIONAL
Enrollment
93
Patient-specific posterior stabilized total knee replacement and patient specific surgical jigs
Tennessee Orthopaedic Alliance
Nashville, Tennessee, United States
Scott Orthopedic Center
Huntington, West Virginia, United States
Demographics and Medical History
Demographics and medical history gathered from medical records
Time frame: 1 year
Pre and Post Operative Range of Motion
Collected retrospectively through medical records, collecting range of motion from pre-operative visits and post-operative visits
Time frame: 1 year
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