sedation and nausea & vomiting during spinal anesthesia in cesarean section. Failed moderate sedation during procedure
Conditions
Interventions
Intervention 1: Intervention group: : The amount of 0.2 mg/kg Propofol 1%(10mg/ml and made by B.BRAUN company in Germany), is injected intravenously after spinal anesthesia by anesthesiologist. Interv
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 46 Years
Inclusion criteria
Inclusion criteria: 18-45 aged pregnant women for C/S ASA CLASS 1, 2 Satisfaction to participate in the project 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 Emergency Cesarean Eclampsia and Preeclampsia Multiple pregnancy Spinal anesthesia contraindications (high ICP, hypovolemia, anemia, coagulation disorders, etc.) History of allergy to eggs, soy, midazolam and propofol Use of antiemetic drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sedation. Timepoint: We record ramsy sedation score in 24 hours after surgery.?. Method of measurement: Ramsy sedation score.;Nausea & vomiting. Timepoint: After surgery. Method of measurement: Observation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Systolic and Diastolic Blood Pressure. Timepoint: Every 5 minutes (from drug administration until end of surgery). Method of measurement: Non-invasive automatic barometric device.;Heart Rate. Timepoint: Every 5 minutes (from drug administration until end of surgery). Method of measurement: Using a pulse oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNahid Manouchehrian
Hamedan University of Medical Sciences
Outcome results
None listed