This study is designed to monitor long term clinical outcomes of the iUni G2+ unicompartmental knee replacement
The study subjects will be followed for 10 years post implant. The follow-up visit schedule will include visits at 6 weeks, 6 months, 1 year, 2 years, 5 years and 10 years post implant.
Study Type
OBSERVATIONAL
Enrollment
28
The iUni G2+ Unicompartmental Resurfacing Device (iUni) is an FDA cleared and CE Marked implant designed for patients with damage isolated to either the medial or lateral tibiofemoral compartment of the knee. The patient-specific iUni is designed from a CT scan of an individual patient's knee using a design process which interactively maps the diseased area and defines the extent of misalignment present in the knee. This process allows definition of the shape and size of the femoral and tibial components of the implant, as well as the disposable instrumentation (Fitz).
The London Clinic
London, United Kingdom
2011 Knee Society Score
Time frame: 1 Year
KOOS Score
Time frame: 1 Year
Oxford Knee Score
Time frame: 1 Year
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