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Long-Term Outcome of Split Laminectomy for Cervical Spondylotic Myelopathy

Long-Term Outcome of Split Laminectomy for Cervical Spondylotic Myelopathy - Cervical split laminectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON44400
Enrollment
100
Registered
2016-05-12
Start date
2016-04-01
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical spondylotic myelopathy

Interventions

None listed

Sponsors

Sint Lucas Andreas Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients who underwent a cervical split laminectomy because of cervical myelopathy between 1 01-01-2005 and 31-12-2014 in OLVG-west (formerly Sint Lucas Andreas Ziekenhuis) are considered for inclusion in this study. To be eligible to participate, a subject must meet all of the following criteria: 1. Male and female subjects aged 18 - 80 years at the time of surgery 2. Subject was diagnosed with cervical myelopathy from degenerative spinal disease requiring posterior surgical decompression 3. Cervical Split Laminectomy was performed between 2004 and 2013 4. Radiological diagnosis was in accordance with clinical signs and symptoms 5. Medical records and radiological images are available for review. 6. Subject is able and willing to comply with the study protocol 7. Subject is able to provide written informed consent

Exclusion criteria

Exclusion criteria: 1. No split but conventional laminectomy was performed 2. Medical records or radiological images are not available 3. Subject underwent previous neck operations 4. Subject underwent surgery for other indications than spondylotic (degenerative) myelopathy, e.g. trauma, tumor, infection 5. Additional posterior fusion and fixation was performed in the same session 6. Subject had a congenital deformity of the cervical spine, e.g. Klippel-Feil or achondroplasia 7. Subject had significant concomitant neurological disease, e.g. severe polyneuropathy or neurodegenerative disease 8. Subject has died 9. Subject cannot be contacted

Design outcomes

Primary

MeasureTime frame
Primary study parameters are the occurence of cervical kyphosis and segmental instability on a cervical radiograph performed at least 2 years after surgery.

Secondary

MeasureTime frame
Secondary study parameters include the Neck Disability Index, the Nurick score the Japanes Orthopaedic Association score and perceived recovery on a 5-point Likert scale.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)