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Optetrak Posterior Stabilized Versus Optetrak Hi-Flex

Arthropathy of Knee Clinical Trial

Official title:
Prospective, Single-center, Non-randomized, Consecutive Series Study Comparing Functional Differences Between a Standard Posterior Stabilized TKR and a High-flexion Posterior Stabilized TKR

Clinical Trial Summary

The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs.

Clinical Trial Description

The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs. The null hypothesis is that there is no difference in postoperative knee flexion between the Optetrak® PS and Optetrak® HF groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00808613
Study type Interventional
Source Exactech
Contact
Status Withdrawn
Phase N/A
Start date December 2008
Completion date January 2012
View Details
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