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Does the design of the cervical disc prothesis and the ancoring mechanism have an influence on the clincial results or the incidence of heterotopic ossifications

Conditions
M42.12
M50.1
Cervical disc disorder with radiculopathy
Registration Number
DRKS00015479
Lead Sponsor
Schön Klinik München Harlaching
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

Implantation of a total cervical disc replacement ProDisc C or ProDisc vivo 1-3 segments

Exclusion Criteria

no matched pair found

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of heterotopic ossifications at the 2 years follow up
Secondary Outcome Measures
NameTimeMethod
clinical results (VAS, NDI, implant related complications)
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