Effect of intravenous palonosetron on hypotension induced by spinal anesthesia for cesarean section: a randomized controlled trial
Not Applicable
Completed
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0006966
- Lead Sponsor
- Chung-Ang Univerisity Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 54
Inclusion Criteria
Single-pregnancy mother aged 18 to 65 undergoing elective cesarean section under spinal anesthesia
Exclusion Criteria
Under 18 years old, over 65 years old, weight 45 kg or less, 100 kg or more, ASA 3 or more, patients with brain or psychiatric disorders or taking related drugs, patients with severe cardiovascular, kidney, liver, or hematologic abnormalities, emergency cesarean section, gestational hypertension, pre-eclampsia, eclampsia, mothers with pregnancy-related complications such as placenta previa, multiple-pregnancy, malformation in the fetus or when a very low birth weight infant weighing less than 1500 g is expected, when a patient refuses spinal anesthesia
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total amount of phenylephrine used until the time of infant delivery
- Secondary Outcome Measures
Name Time Method Presence of side effects of spinal anesthesia such as hypotension, bradycardia, and/or shivering;Outcome variables for cesarean section such as APGAR score and operation time ;Outcome variables for main effects and side effects of experimental drugs such as nausea and vomiting