Actively Recruiting

Age: 18Years - 74Years
All Genders
NCT06886802

Multicentric Case Series of Uniportal Endoscopic Posterior Cervical Decompression for Cervical Spinal Stenosis

Led by TecSalud Investigación Clínica · Updated on 2026-03-04

50

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

Sponsors

T

TecSalud Investigación Clínica

Lead Sponsor

T

Tecnologico de Monterrey

Collaborating Sponsor

AI-Summary

What this Trial Is About

Cervical spinal stenosis is a condition that can cause pain, sensory disturbances, and motor deficits due to the compression of neural structures in the cervical spine. While conservative treatments such as physical therapy and pain management can help some patients, others with persistent neurological deficits may require surgical intervention. Traditional surgical approaches, including anterior decompression and posterior open surgery, have proven effective but carry risks such as vascular or nerve injuries and postoperative pain. This study evaluates a minimally invasive surgical approach called Posterior Uniportal Endoscopic Cervical Decompression as an alternative to traditional methods for patients with cervical spinal stenosis. The main objective is to assess changes in neurological deficits and disability related to cervical pain following this procedure. The study will also document hospitalization duration, surgical time, blood loss, and the incidence of postoperative complications. This multicenter, prospective case series will recruit 50 patients from three medical centers in Mexico. Participants must have symptomatic cervical spinal stenosis that persists despite at least three months of conservative treatment. Eligible patients will undergo Posterior Uniportal Endoscopic Cervical Decompression, a technique that allows precise nerve decompression through a small incision, minimizing damage to surrounding tissues. Standardized clinical assessment tools, including the modified Japanese Orthopaedic Association (mJOA) scale, Neck Disability Index (NDI), and Visual Analog Scale (VAS) for pain, will be used to evaluate outcomes at multiple time points over 12 months. By comparing patients' preoperative and postoperative evaluations, the study aims to determine whether Posterior Uniportal Endoscopic Cervical Decompression effectively improves neurological function and reduces disability while maintaining a favorable safety profile. Findings from this study could support the adoption of minimally invasive endoscopic techniques as a viable option for treating cervical spinal stenosis, potentially leading to faster recovery times and reduced surgical complications compared to traditional methods.

CONDITIONS

Official Title

Multicentric Case Series of Uniportal Endoscopic Posterior Cervical Decompression for Cervical Spinal Stenosis

Who Can Participate

Age: 18Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent to participate in the study
  • Cervical canal stenosis grade I-III according to the Kang scale
  • Presence of radicular or myelopathic symptoms
  • Completed at least 3 months of conservative treatment including physical therapy and analgesics
  • Chosen to undergo posterior uniportal endoscopic cervical decompression for cervical canal stenosis
Not Eligible

You will not qualify if you...

  • Unable to read or write
  • Previous cervical surgery at the treatment levels
  • Presence of infectious symptoms or rheumatologic diseases
  • Cervical vertebral instability
  • Congenital spinal malformations
  • Disc herniation at the same cervical level to be operated on
  • Medullary hyperintensity on T2-weighted MRI at the treatment level(s)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hospital Zambrano Hellion, TecSalud

San Pedro Garza García, Nuevo León, Mexico, 66278

Actively Recruiting

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Research Team

► Mario Benvenutti Regato, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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