caesarean section. Delivery by elective caesarean sectio
Conditions
Interventions
Intervention 1: Patients in group (A) (n=100) received 1 mg/kg in 5 cc normal saline Aminophylline after clamping the umbilical cord and A’ syringe before performing spinal. Intervention 2: Patients i
Treatment - Drugs
Patients in group (A) (n=100) received 1 mg/kg in 5 cc normal saline Aminophylline after clamping the umbilical cord and A’ syringe before performing spinal.
Patients in group (B) (n=100) received 0.15 mg/kg in 5 cc normal saline Ondansetron before performing spinal and B’ syringe after clamping the umbilical cord.
In the control group(C) (n=100) patients received C, C’ syringe 5 cc normal saline after clamping the umbilical and before performing spinal as placebo.
Sponsors
Vice Chancellor for Research, Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: women undergoing elective cesarean section under spinal anesthesia ASA class II- I. Exclusion criteria: pregnant women; heart disease; chronic liver and kidney failure; migraine headaches and stress; chronic hypertension; gestational hypertension; pre-eclampsia; seizures; psychiatric problems; allergy to ondansetron; aminophylline and theophylline; history of drug addiction; failed to spinal anesthesia or more than once spinal anesthesia attempts.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache. Timepoint: every 72, 48, 24 hours in 3 days after surgery. Method of measurement: Numerical rating scale (NRS).;Nausea and vomiting. Timepoint: every 72, 48, 24 hours in 3 days after surgery. Method of measurement: Observasion. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSanaz Bayani
Shiraz University of Medical Sciences
Outcome results
None listed