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Clinical Trial Summary

The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of the Vanguard™ Complete Knee System.


Clinical Trial Description

This is a 10-year prospective observational data collection on the Vanguard Total Knee system. Patients are asked to come in for a preop, operative, immediate post-operative, 6 Month, 1 Year, 3 Year,5 Year, 7 year, and 10 year visits to check on the function, range of motion, and radiographic assessment of their total knee device. The Vanguard Knee is an FDA cleared device, and has been on the market since 2004. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00698854
Study type Observational
Source Zimmer Biomet
Contact
Status Active, not recruiting
Phase
Start date March 2004
Completion date January 2026

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