The randomized study about pain relief after spinal surgery with the conduction block of dorsal rami with Ropivacai
Not Applicable
- Conditions
- umbar spinal stenosis (LSS) Cervical spondylotic myelopathy (CSM)
- Registration Number
- JPRN-UMIN000018702
- Lead Sponsor
- Osaka City Graduate school of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 280
Inclusion Criteria
Not provided
Exclusion Criteria
These patients are excluded 1) Coexisting malignant tumors 2) Pyogenic spondylitis 3) Severe hepatic disorders 4) Severe renal disorders 5) Cardiac conduction abnormalities 6) Allergic history of the ropivacain 7) Lactating women 8) Received ropivacain within 3 months before our injection 9) Received IVH perioperatively 10) Anyone who disqualified by the doctor in charge
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method