Ireland
--:--IST
Recruiting Not applicable

Fusion or no Fusion After Decompression of the Spinal Cord in Patients With Degenerative Cervical Myelopathy

NCT04936074 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2022-02-21
Last updated
2025-04-08

Condition(s) studied

Cervical Spondylotic Myelopathy

Investigational drug(s) / intervention(s)

Muscle preserving selective laminectomyLaminectomy with instrumented fusion

Muscle preserving selective laminectomy: Muscle-preserving selective laminectomy differ from traditional laminectomy by the spinous process split that preserves the deep extensor muscles. The bilateral facet joints are not exposed. After the laminectomy is finished the split fragments of the spinous process are sutured together so that the deep extensor muscles are restored.

Laminectomy with instrumented fusion: A traditional laminectomy is complemented with lateral mass and/or pedicle screws connected with rods.

Study summary

Background:

Degenerative cervical myelopathy (DCM) is characterized by neck pain, neck stiffness, weakness, paresthesia, sphincter disturbance and balance disorder. The mean age for symptoms is 64 years and more men than women, 2.7:1, are affected. The most common level is C5-C6. DCM is the predominant cause of spinal cord dysfunction in the elderly worldwide. Surgical options include stand-alone laminectomy, laminectomy and fusion and laminoplasty. The preferable surgical approach is though, a matter of controversy. The objective of this study is to compare stand-alone laminectomy to laminectomy and fusion.

Methods/Design:

This is a multicenter randomized, controlled, parallel group non-inferiority trial. A total of 300 adult participants are allocated in a ratio of 1:1. The primary endpoint is reoperation for any reason within 5 years of follow-up. Sample size and power calculations were performed by estimating the reoperation rate after laminectomy to 3.4% and after laminectomy with fusion to 7.9% based on data from the Swedish spine registry (Swespine) on patients with DCM.

Secondary outcomes are the patient derived modified Japanese orthopaedic association (P-mJOA) score, Neck disability index (NDI), European quality of life five dimensions (EQ-5D), Numeric rating scale (NRS) for neck and arm pain, Hospital anxiety and depression scale (HADS), development of kyphosis measured as the cervical sagittal vertical axis (cSVA) and, death. Clinical and radiological follow-up is performed at 3, 12, 24 and 60 months after surgery. The main inclusion criteria is 1-4 levels of DCM in the subaxial spine, C3-C7, with or without deformity. The REDcap will be used for safe data management. Data will be analyzed in the per protocol (PP) population, defined as randomized patients who are still alive without having emigrated or left the study after five years.

Discussion:

This will be the first randomized controlled trial comparing two of the most common surgical treatments for DCM; the posterior muscle-preserving selective laminectomy and posterior laminectomy with instrumented fusion. The results of the MyRanC study will provide surgical treatment recommendations for DCM. This may result in improvements in surgical treatment and clinical practice regarding DCM.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \>18 years * 1-4 levels of cervical degenerative myelopathy in the subaxial spine, C3-C7, without or with deformity not exceeding exclusion criteria, see below. * Eligible for both treatments * Ability to understand and read Swedish language * Symptomatic myelopathy with at least one clinical sign of myelopathy * No previous spine surgery * Psychosocially, mentally, and physically able to fully comply with this protocol, including adhering to scheduled visits, treatment plan, completing forms, and other study procedures * Personally, signed and dated informed consent document prior to any study-related procedures, indicating that the patient has been informed of all pertinent aspects of the trial * Definition of kyphosis - cSVA \> 40 mm and/or C2-C7 Cobb \> 10° kyphosis. Definition of spondylolisthesis - anterior slippage of \> 2 mm on cervical radiographs taken in the neutral position. Exclusion Criteria: * Local kyphosis; a modified K-line minimum interval distance (INT) of \<4 mm * Spondylolisthesis \>4 mm and simultaneous translation \>2 mm on lateral flexion/extension radiographs * Soft disc herniations only (no signs of osteophyte formation and hypertrophy of the ligamentum flavum) * Active infection * Neoplasm * Trauma * Inflammatory disease (i.e., rheumatoid arthritis or ankylosing spondylitis or DISH) * Systemic disease including HIV * Lumbar or thoracic spinal disease to the extent that surgical consideration is probable or anticipated within 6 months after the cervical surgical treatment (significant lumbar stenosis as defined by Schizas C or worse). * OPLL * Parkinson´s disease * Drug abuse, dementia, or other reason to suspect poor adherence to follow-up * Previous cervical spine surgery

Primary outcome measure(s)

  • The primary endpoint will be reoperation for any reason to reflect whether laminectomy alone or laminectomy with instrumented fusion results in fewer reoperations without increasing the frequency of complications. — Recorded at 5 years of follow-up
    Reoperation will be considered in case of: * Postoperative hematoma or reperfusion injury with neurologic deterioration within hours/days after the primary surgery. * Change in sagittal alignment (kyphosis, DJK of more than 40 mm cSVA and/or C2-C7 Cobb \< -10°) with corresponding symptoms of camptocormia/increased pain/neurological deterioration. * ASP defined as degenerative changes on an adjacent level diagnosed with MRI and concomitant symptoms of myelopathy and/or radiculopathy. * Implant failure (clear radiolucency around \>1 screw or rod breakage with increased neck pain and/or neurologic deterioration). * Postoperative infection that requires revision surgery.

Trial sites (1)

FacilityCityRegionStatus
Academic Hospital of Uppsala Uppsala Sweden Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04936074 on ClinicalTrials.gov ↗ ← All trials in Sweden