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Clinical Trial Summary

The purpose of this study is to evaluate the clinical functional results of the Triathlon All-Polyethylene Tibia Knee Device.


Clinical Trial Description

After being informed about the study, all patients giving written consent will undergo a screening period to determine eligibility for the study. If eligibility is met, data will be obtained retrospectively from the medical records from the preoperative to shortly after surgery time period. Thereafter, the subject will be evaluated at their 5-year and 10-year post surgery anniversary date. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04636190
Study type Interventional
Source Stryker Orthopaedics
Contact Rushal Parikh
Phone 201-745-0310
Email rushal.parikh@stryker.com
Status Recruiting
Phase N/A
Start date July 2, 2021
Completion date December 2028

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