Comparison of the plasma levobupivacaine concentrations after ultrasound-guided paravertebral block and paravertebral lamina technique.
Not Applicable
- Conditions
- Breast surgery
- Registration Number
- JPRN-UMIN000021759
- Lead Sponsor
- tional hospital organization Tokyo medical center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Exclude criteria are the patients who have local anesthetic allergy or peripheral neuropathy or coagulation abnormality liver dysfunction(child-pugh score>B), renal dysfunction (eGFR<60)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The time course of the levobupivacaine concentration
- Secondary Outcome Measures
Name Time Method