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Clinical Trial Summary

This study will evaluate whether design features of one implant design allows more knee bend than the other. Patients will have 1 design in the left knee and 1 design in their right knee. Both knee surgeries will be on the same day.


Clinical Trial Description

The primary objective of this study is to determine whether the passive, non-weight-bearing flexion is superior with the posterior-stabilized PFC® Sigma™ RP-F compared to the posterior-stabilized PFC® Sigma™ RP in bilateral Subjects receiving both implants and if this difference is a function of implant design. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00380861
Study type Interventional
Source DePuy Orthopaedics
Contact
Status Completed
Phase N/A
Start date March 1, 2006
Completion date December 1, 2009