Correlation Between Parameters and Prognosis of Cervical Single Open-door Surgery

Air Force Military Medical University of People's Liberation Army

Status: Enrolling

Conditions: Cervical Spinal Stenosis

Treatments: Procedure: cervical single open-door surgery

Study type: Interventional

Funder types: Other

Identifiers

NCT05767164

KY20222157-C-1

Details and patient eligibility

About

The aim of study was evaluated the relationship between the relevant evaluation indexes of cervical spine open-door surgery, prognosis and complication rate, and provided theoretical basis for personalized surgical program through multi-center retrospective clinical study

Enrollment: 500 estimated patients

Sex: All

Ages: 18 to 86 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Symptoms and signs of the patients were typical. MRI showed single or multiple central herniation of C3-C7 intervertebral discs or spinal stenosis at corresponding levels, which confirmed cervical myeloid cervical spondylosis or cervical spinal stenosis.
• Conservative treatment for more than 3 months before surgery was ineffective.
• The patients underwent cervical single open-door surgery.
• Informed consent was obtained from the patient and his family, informed consent was signed, and a complete follow-up was completed after surgery

Exclusion criteria

• Cervical spondylotic radiculopathy.
• Cervical kyphosis or instability.
• Cervical spondylosis caused by trauma, tumor, tuberculosis and metabolic diseases.
• Revision surgery or combined anterior-posterior surgery is required.
• The patients had severe neurological diseases affecting the evaluation of postoperative results.
• Psychopath.
• MRI or CT for contraindications.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Double Blind

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500 participants in 4 patient groups

Preoperative

No Intervention group

postoperative (3 months)

Experimental group

Treatment:

Procedure: cervical single open-door surgery

postoperative (6 months)

Experimental group

Treatment:

Procedure: cervical single open-door surgery

postoperative (1 year)

Experimental group

Treatment:

Procedure: cervical single open-door surgery