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A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement System

Osteoarthritis of the Knee Clinical Trial

Official title:
A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement System

Clinical Trial Summary

This study is designed to observe the long term clinical outcomes of patient-specific knee arthroplasty in patients with osteoarthritis.

Clinical Trial Description

If the patient has previously received a standard total knee replacement in their contralateral knee, the primary endpoint questionnaire and some secondary endpoint questionnaires will be completed regarding BOTH their iTotal® CR knee and their standard total knee for all time points where questionnaires are required by the protocol. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01820650
Study type Observational
Source Restor3D
Contact
Status Terminated
Phase
Start date February 2013
Completion date October 2023
View Details
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