cesarean. Newborn (suspected to be) affected by Cesarean delivery
Conditions
Interventions
Intervention 1: Interventional group: patients in the first group receive 8 mg dexamethasone in 100 cc normal saline via micro set and three way in 15 minutes. Intervention 2: Intervention group:Pati
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: ASA I-II Minimum NPO time = 8 hours Elective cesarean section
Exclusion criteria
Exclusion criteria: Spinal anesthesia Contraindications of Local infection in the lumbar region (spinal cord needle entry site) Use anti-platelet and anticoagulant Sensitivity to Local anesthesia Diabetes mellitus kidney Diseases Renal failure Coagulation disorder Liver disease Heart disease History of seizure or any neurological disease Migraine and pressure headaches The history of drug addiction Failure of spinal anesthesia or multiple attempts to perform spinal anesthesia more than once Systolic blood pressure above 150 and less than 100 Preeclampsia IUGR The lack of proper growth of the uterus Weight above 100 Height less than 150 and more than 180 cm Hemoglobin less than 8 Caesarean section more than 3 times Sensitivity to dexamethasone and paracetamol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache. Timepoint: At the arrival to the recovery room and after discharge from the recovery room at 6,12,24,48,72 hr. Method of measurement: Visual Analog Score. | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of Nausea and Vomiting. Timepoint: At the arrival to the recovery room and after discharge from the recovery room at 6,12,24,48,72 hr. Method of measurement: Observasion. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Hosein Pourjafarian
Shiraz University of Medical Sciences
Outcome results
None listed