Comparison of the plasma levobupivacaine concentrations after ultrasound-guided transversus abdominis plane block and rectus sheath block.
Not Applicable
- Conditions
- laparoscopic surgery
- Registration Number
- JPRN-UMIN000013115
- Lead Sponsor
- ational 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 liver dysfunction (child-Pugh Score>B) or renal dysfunction (eGFR<60), history of local anesthetic allergy.
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