Spinal anesthesia in cesarean section. Single liveborn infant, delivered by cesarean
Conditions
Interventions
Intervention 1: Intervention group: 0.5 mg of atropine is injected intravenously after spinal anesthesia. Intervention 2: Control group: 1 ml of normal saline is injected intravenously immediately aft
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
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 Multiple pregnancies HR resting more than 100 in minutes, Beta-blocker intake
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.;Bradycardia. 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: Pulse Oximetry. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea & vomiting. Timepoint: after delivery. Method of measurement: Observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNahid Manouchehrian
Hamedan University of Medical Sciences
Outcome results
None listed