Comparative study of clinical and radiological outcomes of anterior cervical discectomy and fusion using ceramic cage or PEEK cage: a prospective randomized controlled trial.
- Conditions
- Diseases of the musculoskeletal system and connective tissue
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 60
? Symptoms and signs of radiation to one or both arms (pain, dyspnea, or paralysis according to the distribution of a particular neuromuscular muscle) or symptoms and signs related to acute or chronic spinal cord disease
? At least 8 weeks of conservative treatment (physical therapy, pain medication)
? Imaging diagnoses of cervical intervertebral valve dislocation and (or) osteoclastic formation in one or two segments associated with clinical symptoms and signs (from cervical spine 3-4 to cervical spine 7 to thoracic spine 1) are possible
? who want to participate in clinical research
? with prior written consent from the patient or his/her legal representative
? Uncertain or ambiguous symptoms
? previous history of anterior or posterior access cervical spine surgery
? If there is a risk of instability due to a height difference of more than 3 mm in simple radiographic examination of extension and flexion
? Severe post-chronic symptoms in the segment (above 7 degrees)
? Patient fails to take MRI
? Who has cervical pain without radiating symptoms or spondylosis
? In the presence of an infectious disease
? In the case of metabolic diseases such as severe osteoporosis or bone diseases
? Who has a tumor or trauma to your cervical spine
? Who has deformity of the spine
? Who has a severe mental illness
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method