Patients who underwent orthopedic artificial joint surgery under general anesthesia
Conditions
Interventions
Patients received intravenous ondansetron 4 mg, receiving postoperative analgesia with continuous epidural infusion.
Patients received intravenous ondansetron 4 mg, receiving intraoperative periarticu
Sponsors
Tokushima University Graduate School
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients, ASA I-III, who underwent orthopedic artificial joint surgery under general anesthesia.
Exclusion criteria
Exclusion criteria: Patients over ASA IV. Patients who do not obtain the consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative nausea and vomoting Pain VAS:Visual analog scale | — |
Countries
Japan
Contacts
Public ContactNami KAkuta
Institute of Biomedical Sciences Tokushima University Graduate School Department of Anesthesiology
Outcome results
None listed