None listed
Conditions
Interventions
Drug : We randomly assinged into 2 groups, administering palonosetron0.075mg or no prophylaxis(placebo administration).In patients undergoing both knee arthroplasty, there was one-week interval betwee
Sponsors
Seoul National University Bundang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients undergoing total knee arthroplasty who understands the study design and voluntarily agrees with the study.
Exclusion criteria
Exclusion criteria: Patients who are contraindicated to spinal anesthesia,did not administered iv-PCA or femoral nerve block, undergoing steroid therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative nausea and vomiting(PONV) | — |
Secondary
| Measure | Time frame |
|---|---|
| rescue antiemetics | — |
Countries
Korea, Republic of
Contacts
Public ContactHye-min Sohn
Seoul National University Bundang Hospital
Outcome results
None listed