Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age28-85
SponsorXijing Hospital
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.
Eligibility criteria
Qualifiers
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 routine tests and examinations.
Informed consent of patients.
Disqualifiers
Cervical radiculopathy
Cervical kyphosis or instability
Cervical spondylosis caused by trauma, tumor, tuberculosis and metabolic diseases
Revision surgery or combined anterior-posterior surgery is required
Trial design
Treatments tested in this trial
- Centerpiece titanium plate
Treatment groups
500 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov