Spinal anesthesia. Other complications of spinal and epidural anesthesia during pregnancy
Conditions
Interventions
Intervention 1: The intervention group will receive 7 ml/kg of ondansetron intravenously before the start of spinal. Intervention 2: The control group will receive 7 ml/kg of normal saline intravenous
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 37 Years
Inclusion criteria
Inclusion criteria: Pregnant women aged between 18 -37 years Female candidates for cesarean delivery and spinal anesthesia
Exclusion criteria
Exclusion criteria: Neurological disorders Injection site infection Liver Disease and BMI> 30
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: Immediately after Spinal, every 3 minutes to 30 minutes. Method of measurement: Using the barometer device.;Nausea and vomiting. Timepoint: The beginning and the end of the study. Method of measurement: Asking of patient.;Headache. Timepoint: The beginning and the end of the study. Method of measurement: Ask the patient.;Chill. Timepoint: The beginning and the end of the study. Method of measurement: Asking of patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahin Molaei
Kermanshah University of Medical Sciences
Outcome results
None listed