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Clinical Trials/CTRI/2025/12/098987
CTRI/2025/12/098987RecruitingNot Applicable

Does Preservation of C2 and C7 Spinous Process Attachments Improve Patient Outcomes in Cervical Laminectomy? A Prospective Observational Study

Stavya Spine Hospital and Research Institute1 site in 1 country200 target enrollmentStarted: December 24, 2025Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
mJOA scores (0-18): Assessed preoperatively and at 3, 6, 12, and 24 months postoperatively. JOA recovery rate calculated using: Recovery Rate (%) = [(Postoperative JOA - Preoperative JOA) / (17 - Preoperative JOA)] × 100.

Study Overview

Brief Summary

This prospective observational comparative study will be conducted at Stavya Spine Hospital and Research Institute, Ahmedabad. The study enrolled 200 consecutive patients diagnosed with multilevel cervical spondylotic myelopathy (CSM) requiring cervical laminectomy at C3-C6 or C3-C7 levels. Patients will be prospectively distributed into two equal groups based on the surgical technique employed at the time of surgery: Group A (Preservation Group, n=100) which will undergo modified muscle-preserving laminectomy with preservation of semispinalis cervicis and nuchal ligament attachments at C2 and C7 spinous processes, while Group B (Conventional Group, n=100) will undergo conventional laminectomy with complete detachment of the posterior muscle complex from C2 and C7 spinous processes. Written informed consent was obtained from all participants prior to surgery.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
40.00 Year(s) to 75.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • •Multilevel cervical stenosis involving greater or equal to 3 consecutive levels
  • •Symptomatic cervical myelopathy with clinical and radiological correlation.

Exclusion Criteria

  • •Documented history of prior cervical spine surgery.
  • •Congenital spinal anomalies.
  • •Individuals with inflammatory arthropathies.
  • •Individuals with a history of traumatic injury to the cervical spine.
  • •Individuals with significant comorbidities that may interfere with treatment outcomes (e.g., severe osteoporosis, malignancies, or systemic inflammatory disorders).
  • •Ossification of Posterior Longitudinal Ligament (OPLL) extending beyond C2 and/or C
  • •Inability to comply with the follow up schedule.
  • •Pathology extending beyond C2 and/or C7.

Outcomes

Primary Outcomes

mJOA scores (0-18): Assessed preoperatively and at 3, 6, 12, and 24 months postoperatively. JOA recovery rate calculated using: Recovery Rate (%) = [(Postoperative JOA - Preoperative JOA) / (17 - Preoperative JOA)] × 100.

Time Frame: Follow up visits at 3 months, 6 months and 1 year

Visual Analogue Scale (VAS) for axial neck pain : Measured at all time points, with 0 indicating no pain and 10 indicating worst imaginable pain.

Time Frame: Follow up visits at 3 months, 6 months and 1 year

Neck Disability Index (NDI) (0-50 scale or percentage): Assessed at all time points, evaluating functional disability related to neck pain.

Time Frame: Follow up visits at 3 months, 6 months and 1 year

Cervical Range of Motion (ROM) (degrees): Measured on dynamic lateral radiographs at 12 postoperatively.

Time Frame: Follow up visits at 3 months, 6 months and 1 year

Secondary Outcomes

  • C2-C7 Cobb angle (degrees): Measured on lateral cervical radiographs at preoperative baseline & 12 months postoperatively.(C2-C7 sagittal vertical axis (SVA) (mm): Measured on lateral cervical radiographs at baseline & 12 months.)

Investigators

Sponsor
Stavya Spine Hospital and Research Institute
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Dr Bharat R Dave

Stavya Spine Hospital And Research Institute

Study Sites (1)

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