CompletedNot Applicable

Quintex® Follow-up After One Year Minimum

Germany60 participantsStarted 2019-11-11

Plain-language summary

Prospective study, not randomised, non-interventional, monocentric, investigating an intended patient cohort of 60 patients already operated on the cervical spine due to degenerative disc disease of the cervical spine down to the first thoracolumbar VBR (C2-T1), who received a Quintex plate for stabilisation

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- all patients who received a Quintex® Anterior Cervical Plate since 2014 until approx. end 2018 (minimum Follow-up is one year) in the study center Exclusion Criteria: * Patient informed consent not signed * Patients living outside a radius of 80 km around the study center

What they're measuring

Clinical Results measured by Neck Disability Index (NDI)

Timeframe: One retrospective visit, between one and approx. five years post-op.

Trial details

NCT IDNCT04489394

SponsorAesculap AG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2020-02-18

View on ClinicalTrials.gov More Degenerative Disc Disease trials