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Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical — CERISE  

Degenerative Disc Disease Clinical Trial

Official title:
Multicenter Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical - a Prospective Study on Total Indications

Clinical Trial Summary

Multicenter Post market clinical follow-up Study on the Safety and Performance of Ennovate® Cervical - Prospective, pure data collection of all Ennovate Cervical patients in Total Indications

Clinical Trial Description

This clinical study is one of the Post market clinical follow-up measures that enables the manufacturer to monitor the clinical safety and performance of the Ennovate® Cervical system. The study enables a quick, but detailed implant documentation, which is of great interest for the current and future users of the internal fixation system targeted in this study. It includes the relevant outcomes to evaluate safety and efficacy of the implant system for various indications in trauma and degenerative disorders. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05296889
Study type Observational
Source Aesculap AG
Contact Sarah Mattes
Phone +497461950
Email sarah.mattes@aesculap.de
Status Recruiting
Phase
Start date July 21, 2021
Completion date December 2025
View Details
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