Actively Recruiting
Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
Led by Xijing Hospital · Updated on 2025-04-09
500
Participants Needed
1
Research Sites
148 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the safety and effectiveness of individualized, precise and standardized open-door posterior cervical surgery through a single-center, exploratory clinical study, so as to provide a more reliable basis for the treatment of cervical spinal stenosis.
CONDITIONS
Official Title
Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 28 and 85 years old
- Diagnosed with C3-7 multilevel cervical spondylitis myelopathy or cervical spinal stenosis requiring posterior cervical open-door surgery
- No contraindications found in preoperative routine tests and examinations
- Provided informed consent to participate in the study
You will not qualify if you...
- Diagnosis of cervical radiculopathy
- Presence of cervical kyphosis or instability
- Cervical spondylosis caused by trauma, tumor, tuberculosis, or metabolic diseases
- Need for revision surgery or combined anterior-posterior surgery
- Serious neurological diseases affecting postoperative evaluation
- Mental illness preventing cooperation with follow-up
- Contraindications for MRI examination
- Patient or family does not agree to participate
- Other conditions unsuitable for study participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Qi Wei
Xi'an, Shannxi Province, China, 710034
Actively Recruiting
Research Team
W
Wei Qi
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
TREATMENT
Number of Arms
2
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