patients scheduled for gynecological laparotomy under general anesthesia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.female patients(American Society of Anesthesiologists physical status 1 to 3) undergoing gynecologic laparotomy at Sumitomo hospital 2.Written informed consent is provided
Exclusion criteria
Exclusion criteria: 1.over ASA-PS4 2.epidural anesthesia 3.laparoscopic surgery 4.allergy in ropivacaine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analog scale (VAS) at rest and at mobilization, assessed at 3, 24,48 and 72hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Plasma ropivacaine concentarations before and 16, 40 and 64hours after starting continuous wound infusion 2.Time to independent ambulations 3.Consumption of rescue analgesia at 24,48,72hours after surgery 4.Incidence of nausea and vomitting 5.Ocurrence of local anesthetic intoxication by ropivacaine 6.Ocurrence of adverse effects by cathters placed into the wound | — |
Countries
Japan
Contacts
Sumitomo Hospital Department of Anesthesia