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Signature Personalised Patient Care System With the Vanguard Knee System Study

Arthroplasty, Replacement, Knee Clinical Trial

Official title:
Study on the Signature Personalised Patient Care System With the Vanguard Knee System

Clinical Trial Summary

The purpose of this study is to determine whether the percentage cases which have ideal mechanical axial alignment using the Vanguard total Knee implant with the Signature cutting blocks is higher than those without the use of Signature when measured immediately post-operatively.

Clinical Trial Description

The purpose of this study is to determine whether the percentage cases which have ideal mechanical axial alignment using the Vanguard total Knee implant with the Signature cutting blocks is higher than those without the use of Signature when measured immediately post-operatively. Other outcomes will include knee assessments and patient questionnaires. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01092312
Study type Interventional
Source Zimmer Biomet
Contact
Status Terminated
Phase N/A
Start date March 2010
Completion date September 2016
View Details
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