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Anterior Vs Posterior Procedures for Cervical Spondylotic Myelopathy: Prospective Randomized Clinical Trial

A Comparison of Anterior and Posterior Procedures for the Surgical Management of Cervical Spondylotic Myelopathy: Prospective Randomized Clinical Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00876603
Acronym
CSM
Enrollment
100
Registered
2009-04-07
Start date
2001-05-31
Completion date
2020-12-31
Last updated
2010-01-14

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

Conditions

Cervical Spondylotic Myelopathy

Keywords

cervical spondylotic myelopathy, anterior decompression and fusion, cervical laminoplasty

Brief summary

There is no difference in surgical outcomes for patients suffering from cervical spondylotic myelopathy treated with anterior decompression and fusion or posterior cervical laminoplasty.

Detailed description

Cervical spondylotic myelopathy (CSM) is a syndrome consisting of symptoms and signs of cervical spinal cord compression caused by chronic degenerative changes of the cervical spine. CSM is the most serious and disabling condition of cervical spondylosis. Natural history studies showed that most of the CSM patients have a progressive deterioration course and no spontaneous regression occurs. It is suggested that the patients with moderate to severe CSM should be operated as early as possible before neurological deficits are too pronounced. Although there are many options available for the surgical treatment of cervical spondylotic myelopathy, the choice of surgical approach for CSM is still a controversial issue. Most of the surgeons select the surgical approach based on the number of levels involved and the alignment of the spine. Anterior procedure is generally recommended for patients with compression of less than 3 levels or in patients with kyphotic alignment, while posterior decompression is suggested for three or more levels of compression. Retrospective clinical study however has shown that both anterior and posterior surgeries could produce comparable results. There is no scientific data based on randomized, prospective clinical studies comparing the various surgical alternatives. The existing information does not clearly favor any one single approach or operative option. Since anterior and posterior surgeries carries different risks, it is important to identify the most appropriate surgical procedure that is supported by evidence rather than just by surgeons preference. The objective of this study is to compare the long-term clinical outcome of anterior approach versus posterior approach in the treatment of cervical myelopathy caused by degenerative disease of the cervical spine.

Interventions

PROCEDUREACDF

Anterior cervical decompression and fusion

Cervical laminoplasty

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with transverse lesion type of cervical myelopathy caused by cervical spondylosis requiring surgery. * Involved levels limited to 1, 2 and 3 continuous levels

Exclusion criteria

* Radiculomyelopathy * Cervical kyphosis * Cervical myelopathy caused by high energy trauma * Female \> 70 years old or patients with severe osteoporosis * High anaesthetic risk * Cervical myelopathy other than transverse type * Cervical myelopathy caused by ossification of posterior longitudinal ligament or inter-vertebral disc herniation.

Design outcomes

Primary

MeasureTime frame
Japanese Orthopaedic Association Score for Cervical Myelopathy3 months, 6 months, 1 year, 3 years, 5 years and 10 years

Secondary

MeasureTime frame
Motor and sensory functions, gait and hand functions, neck pain, change in cervical alignment, spinal cord signal change on MRI, operative time, blood loss, duration of in-patient stay, post-operative complication, re-operation rate.3 months, 6 months, 1 year, 3 years, 5 years and 10 years

Countries

China

Contacts

Primary ContactWai Yuen Cheung, MBBS, FRCS
lcheung@hkucc.hku.hk(852) 28554111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026