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Clinical Trial Summary

Prospective, monocenter post market clinical follow-up of a primary knee replacement bearing the CE-mark. 200 subjects will be recruited and followed up for up to ten years or until revision of the primary knee endoprosthesis, whichever occurs first. Documentation of clinical and radiological parameters within the clinical routine pre-operative and post-operative at 3 and 12 months and 2, 5 and 10 years to evaluate time to revision, pain situation, knee functionality, mobility and stability.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02615522
Study type Observational
Source Peter Brehm GmbH
Contact
Status Terminated
Phase
Start date September 2016
Completion date November 2020

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