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Functioning in Individuals with Cervical Radiculopathy After Posterior Cervical Decompression

L

Linköping University (LiU)

Status

Enrolling

Conditions

Cervical Radiculopathy

Treatments

Procedure: Posterior cervical foraminotomy (with our without laminectomy)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Compression on structures, as spinal nerves, in the cervical spine can cause cervical radiculopathy which leads to pain, disability, and reduced quality of life for the affected individual. Cervical foraminotomy with our without laminectomy are common posterior decompression surgical techniques for treating cervical radiculopathy. There is a lack of knowledge regarding function in patients with cervical radiculopathy after posterior cervical decompression.

The aim with this study is to study pain, function, psychosocial factors, and health related quality of life after posterior cervical decompression in patients with cervical radiculopathy.

This is a prospective multicenter longitudinal observational cohort study with follow-up at three, 12- and 24 months postoperative. A total of 154 individuals scheduled to undergo foraminotomy with our without laminectomy due to cervical radiculopathy will be included. Primary outcome is neck-specific function measured with the Neck Disability Index. Data will be collected preoperatively and at three, 12 and 24 months with electronic questionnaire.

Enrollment

154 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cervical radiculopathy, confirmed by MRI images (or alternative neuroradiological imaging if MRI contraindicated) compatible with clinical findings of nerve root compression (neurological examination performed by a neurosurgeon/orthopedic surgeon)
  • Posterior cervical decompression as foraminotomy with our without laminectomy
  • At least 3 months of persistent arm pain
  • Age 18-75 years

Exclusion criteria

  • Nurick score 2 or more (to exclude individuals with moderate to high myelopathy)
  • Previous surgery of cervical spine
  • Previous fracture or dislocation of the cervical spine
  • Malignancy or benign spinal tumor (eg, neuromas)
  • Spinal infection
  • Previous spondylodiscitis
  • Servere mental disorder
  • Known alcohol or drug abuse
  • Lack of ability to write/comprehend/express oneself in Swedish

Trial contacts and locations

3

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Central trial contact

Jard Svensson, MSc

Data sourced from clinicaltrials.gov

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