Clinical trial of custom-made titanium for cervical spine fusio
Not Applicable
- Conditions
- cervical spondylotic myelopathy, cervical disc hernia, cervical ossification of posterior ligamentum flavum, cervical spondylotic radiculopathy
- Registration Number
- JPRN-UMIN000009145
- Lead Sponsor
- Kyoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 8
Inclusion Criteria
Not provided
Exclusion Criteria
1) No lumbar or thoracic spine disease 2) No collagen disease 3) No uncontrolable general disease 4) No malignacy 5) No psychological disease 6) No steroid treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of adverse event and failure. Improvement of preoperative symptoms.
- Secondary Outcome Measures
Name Time Method