Retrospective comparing fusion rate analysis of a TLIF PEEK cage according to the addressed spinal segments.
- Conditions
- Degnerative Discopathie, Postnukleotomiesyndrom, Osteochondrose, Neuroforamenstenose, SpondylolisthesisM40-M54Dorsopathies
- Registration Number
- DRKS00004832
- Lead Sponsor
- Signus Medizintechnik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
age > 18 years
- male and female
- Surgery done with TLIF monosegmental (L4/5 or L5/S1) or bisegmental (L4-S1)
- degenerative disc desease, postnucleotomy syndrome, spondylosis, neuroforaminal stenosis or spondylolisthesis
Exclusion Criteria
- Smoking
- Diabets
- Spondylodiscitis
- Revision Surgery on former TLIF Procedures
- former lumbar interbody fusion in other segments (non L4/5 and L5/S1)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method