None listed
Conditions
Interventions
Drug : Control group receives the intravenous normal saline 2 mL.
Ramosetron group receives the intravenous Ramosetron 2 mL (0.3 mg).
Sponsors
Ajou University Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Laparoscopic cholecystectomy under general anesthesia
Exclusion criteria
Exclusion criteria: BMI > 30 kg/m2, respiratory infection, uncontrolled hypertension
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| optimal Ce of remifentanil | — |
Secondary
| Measure | Time frame |
|---|---|
| complications, emergence time, pain score | — |
Countries
Korea, Republic of
Contacts
Public ContactJi Kim
Ajou University Hospital
Outcome results
None listed