Efficiency and safety of laparoscopic regional anesthesia for abdominal wall in gynecologic laparoscopy: a randomized trial
Phase 3
- Conditions
- Regional anesthesia in gynecologic laparoscopy
- Registration Number
- JPRN-UMIN000014746
- Lead Sponsor
- Department of Obstetrics and Gynecology, University of Occupational Environmental Health, Japan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients weighing less than 50kg 2)Patients with severe disorder of liver function 3)Patients on chronic hemodialysis 4)Patients with clotting abnormality 5)Patients taking anticoagulant and antiplatelet 6)Patients with diabetes mellitus and multiple sclerosis 7)Patients with allergy for regional anesthetic 8)Patients scheduling to undergo single-incision laparoscopy 9)Patients with any difficulty in regional anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluating postoperative pain at 6 hour, 12hour and postoperative days1-3 by Wong-Baker pain scale .
- Secondary Outcome Measures
Name Time Method Evaluating the number of postoperative analgesics.