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Clinical Trial Summary

The study aim is to show the effectiveness of a hybrid system (DTO) regarding clinical outcome and radiological alteration in a single-center prospective setting.


Clinical Trial Description

Posterior spondylodesis and monosegmental intervertebral cage plus flexible instrumentation of the superiorly adjacent segment (Dynesys DTO).

Planned follow-up visits up to 48 months with documentation of health-related outcome measurement instruments and radiological control of possible segment alteration and device-related complication. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03404232
Study type Interventional
Source University Hospital, Aachen
Contact
Status Completed
Phase N/A
Start date January 1, 2012
Completion date December 31, 2017

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