None listed
Conditions
Interventions
Drug : Patients were randomized to receive either ramosetron 0.3 mg, ondansetron 4 mg or ondansetron 8 mg intravenously. Each drug was infused 5 minutes before performing spinal anesthesia.
Sponsors
Seoul National University Bundang Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients undergoing spinal anesthesia
Exclusion criteria
Exclusion criteria: Hypersensitivity on 5-HT3 receptor antagonist uncontrolled hypertension intake of selective serotonin reuptake inhibitor
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The gap between baseline mean arterial pressure and lowest mean arterial pressure measured during 30 min after spinal anesthesia | — |
Secondary
| Measure | Time frame |
|---|---|
| The gap between baseline systolic arterial pressure and lowest systolic arterial pressure measured during 30 min after spinal anesthesia;The gap between baseline diastolic arterial pressure and lowest diastolic arterial pressure measured during 30 min after spinal anesthesia;incidence of postoperative nausea and vomiting | — |
Countries
Korea, Republic of
Contacts
Public ContactHyun-Jung Shin
Seoul National University Bundang Hospital
Outcome results
None listed