Osteoarthritis, Knee Clinical Trial
Official title:
Randomized Controlled Study Comparing iASSIST Knee System Versus Conventional Instrumentation
The purpose of this study is to compare the accuracy of knee component alignment between patients operated with iASSIST Knee (Investigational group) versus patients operated without iASSIST Knee (Control group) using the same implant system.
Objective： To compare the accuracy of knee component alignment between patients operated with
iASSIST Knee (Investigational group) versus patients operated without iASSIST Knee (Control
group) using the same implant system.
Endpoint： Primary： The alignment accuracy of the knee femoral and tibial components at 6
months for the investigational group compared to the control group.
Secondary：Health Status after TKA, Operating Room efficiency and Complication rate after TKA
for the investigational group compared to the control group.
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