Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
Recruiting
N/A
Interventional Study
Cervical Spinal Stenosis
Cervical Spinal Cord Injury
Individuation
Standardization
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 28 – 85
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 500 (estimated)
- Sponsor
- Xijing Hospital · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* The age of 28-85 years old; Through systematic clinical and imaging examination, patients diagnosed with C3-7 multilevel cervical spondylitis myelopathy or cervical spinal stenosis who need to undergo posterior cervical open-door surgery.
* No contraindications in preoperative…
Contacts