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Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee — TriathlonCR  

Total Knee Arthroplasty Clinical Trial

Official title:
Clinical Outcome Study for the Triathlon CR Total Knee

Clinical Trial Summary

An open label, post-market, non-randomised, historical controlled, multi-centre study of the outcomes of the Triathlon Cruciate Retaining (CR) Total Knee System.

Clinical Trial Description

An open label, post-market, non-randomised, historical controlled, multi-centre study of the outcomes of the Triathlon Cruciate Retaining (CR) Total Knee System. The primary objective of this study will be to compare the active range of motion values for the Triathlon CR Total Knee System with those of the Scorpio CR Total Knee System, a historical control group. ROM values will be measured by use of a Goniometer according to the protocol. It is expected that the Triathlon CR Total Knee System group's range of motion is not 5 degrees worse or superior to the control group's range of motion at two-years. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02535741
Study type Interventional
Source Stryker Orthopaedics
Contact
Status Completed
Phase N/A
Start date October 2006
Completion date May 2016
View Details
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