Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hospital Zambrano Hellion, TecSalud
San Pedro Garza García, Nuevo León, Mexico, 66278
Actively Recruiting
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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