Quintex® Follow-up After One Year Minimum

Aesculap

Status: Completed

Conditions: Instability; Back; Degenerative Disc Disease; Deformity of Spine; Cervical Spondylosis; Trauma; Spondylolisthesis; Pseudoarthrosis of Spine; Spinal Stenosis

Study type: Observational

Funder types: Industry

Identifiers

NCT04489394

AAG-O-H-1901

Details and patient eligibility

About

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

Enrollment: 60 patients

Sex: All

Volunteers: No Healthy Volunteers

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