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Spots Global Cancer Trial Database for Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical

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Trial Identification

Brief Title: Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical

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

Study ID: NCT05296889

Study Description

Brief 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

Detailed 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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Krankenhaus Ludmillenstift Meppen, Meppen, Niedersachsen, Germany

Berufsgenossenschaft Klinikum Bergmannstrost Halle / Saale, Halle, Sachsen-Anhalt, Germany

Städtisches Klinikum Dresden, Dresden, Sachsen, Germany

Schön Klinik Hamburg Eilbek, Hamburg, , Germany

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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