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Fully Disposable Patient-Specific Instrumentation — MyKnee  

Osteoarthritis,Knee Clinical Trial

Official title:
Primary TKA Using a Fully Disposable Patient-Specific Instrumentation: A Multicenter Controlled Study

Clinical Trial Summary

To evaluate the lower limb alignment following total knee arthroplasty (TKA) performed with fully disposable patient-specific instrumentation versus conventional, versus patient specific instrumentation.

Clinical Trial Description

The investigators performed a controlled multicenter trial comparing the clinical and radiologic results and resources consumption of primary TKA using patient-specific cutting guides (PSCG) versus conventional instrumentation (CI), and compared the results to those obtained with a fully disposable patient-specific instrumentation (PSCG-D). ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02966613
Study type Interventional
Source Cochin Hospital
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date September 2016
View Details
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