Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
Key facts
- Where
- Xi'an, ChinaSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 28 and 85 years old?
Source: NCT05786313, who can take part
Where in China
- Qi WeiXi'an, ChinaContact: Wei Qi, DoctorTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Xijing Hospital
- Trial code
- NCT05786313
- Record updated
- 30 July 2026
- Original description
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.Read full original descriptionShow less
Prospective Controlled Clinical Study of Individualized, Precise and Standardized Posterior Cervical Open-door Surgery for Cervical Spinal Stenosis
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.
Inclusion: 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.
Exclusion: Revision surgery or combined anterior-posterior surgery is required; Cervical spondylosis caused by trauma, tumor, tuberculosis and metabolic diseases; Serious neurological diseases affect the postoperative effect evaluation; Mental illness cannot cooperate with follow-up; Cervical radiculopathy; Cervical kyphosis or instability; Contraindications for MRI examination; Patients themselves or their families do not agree to participate in the study; Other situations that are not suitable for study participation.