\- Title: PATIENT-MATCHED INSTRUMENTATION VS. STANDARD INSTRUMENTATION: A RANDOMIZED CLINICAL TRIAL COMPARING POSTOPERATIVE AXIAL ALIGNMENT and COMPONENT POSITION * Short Title: Visionaire Alignment * Methodology: Monocentric, Single Blinded, Randomized Controlled Trial * Study Duration: November 2010 to July 2014 * Study Centres: Leicester General Hospital, United Kingdom (UK)
Malalignment is one of the main reasons for knee arthroplasty revision. With the use of patient matched cutting block we expect better axial alignment of the components. Research Objectives: * The primary research objective is to evaluate the axial alignment and component position in TKA with use of Smith \& Nephew's VISIONAIRE Patient Matched Technology and to compare with the alignment when standard instrumentation. * Secondary research objectives include assessing the safety and effectiveness of the VISIONAIRE patient matched technology as compared to commonly accepted standard instrumentation in patients suffering from symptomatic osteoarthritis of the knee joint. \- Outcome Measures: * Implant alignment and Component position by means of CT-scans * Knee Society Score * EuroQol-5 Dimensions (EQ-5D) * Knee injury and Osteoarthritis Outcome Score (KOOS) * Oxford Knee Score * Knee-related adverse events * Standard and full leg x-ray * Number of Subjects: 70 (2\*35) * Enrollment time: 18 months * Diagnosis and Main Inclusion Criteria: Patients with osteoarthritis of the knee requiring total knee arthroplasty * Study Product, Dose, Route, Regimen: VISIONAIRE patient matched technology versus the commonly accepted standard instrumentation for the Genesis II total knee arthroplasty implant
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
70
Implantation of a Genesis II Total Knee by means of Visionaire patient matched cutting blocks.
Implantation of Genesis II Total Knee system by means of standard surgical technique.
Leicester General Hospital
Leicester, United Kingdom
Axial Alignment
Axial alignment will be measured by means of CT scan and long leg x-ray
Time frame: 6 weeks,
Clinical effectiveness and safety.
Safety and effectiveness will be measured by means of Knee Society Score, Oxford Score, EQ-5D and radiographic findings
Time frame: 1 year
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