Regional anesthesia in gynecologic laparoscopy
Conditions
Interventions
Patients randomly are assigned with a 1:1 ratio to receive injection or not. Control group have no regional anesthesia and prescribe oral medicine, suppository and intramuscular injection of analgesic
Sponsors
Department of Obstetrics and Gynecology, University of Occupational Environmental Health, Japan
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1)Patients scheduling to undergo benign gynecologic laparoscopy 2)Female patients older than 19 years 3)Patients who approve our research program and write informed consent
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluating postoperative pain at 6 hour, 12hour and postoperative days1-3 by Wong-Baker pain scale . | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluating the number of postoperative analgesics. | — |
Countries
Japan
Contacts
Public ContactYasuyuki Kinjo
University of Occupational Environmental Health, Japan Department of Obstetrics and Gynecology
Outcome results
None listed