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COREV 2.0 PMCF-Study on Manual and Navigated Revision Knee Patients — COREV  

Knee Osteoarthritis Clinical Trial

Official title:
Comparative, Case Control, Mono-center PMCF Study on Manual and Navigated Revision Knee Patients After a Minimum Follow-Up of Two Years

Clinical Trial Summary

The Columbus® Revision endoprosthetic system is bearing the CE-mark. This means that within the scope of this observational study the patient will not be subjected to any additional stressful, study-related medical examinations or treatment measures. The treatment will be carried out exclusively according to medical standards. The study therefore only serves the purpose of observing this standard-compliant treatment and specifically documenting it scientifically.

Clinical Trial Description

The study's main purpose is the collection of clinical data on the safety and performance of the Columbus® Revision Knee endoprosthesis ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05113303
Study type Observational
Source Aesculap AG
Contact
Status Active, not recruiting
Phase
Start date March 16, 2022
Completion date December 2024
View Details
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