Spinal anesthesia in cesarean section. Single liveborn infant, delivered by cesarean
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Satisfaction to participate in the project Pregnant women aged 18 to 46 Pregnant women who underwent cesarean section under spinal anesthesia
Exclusion criteria
Exclusion criteria: sensitivity to medications used Patients who have failed spinal anesthesia and undergo general anesthesia Lung disease, heart disease, asthma, fever, hypertension, preeclampsia and eclampsia, cardiac arrhythmia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hypotension. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: Non-invasive blood pressure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea & vomiting. Timepoint: after delivery. Method of measurement: Observation.;New born Apgar. Timepoint: 1&5 minutes after delivery. Method of measurement: Apgar Score.;Headache. Timepoint: after delivery. Method of measurement: Observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Hamedan University of Medical Sciences