Spinal anesthesia in cesarean section. Single liveborn infant, delivered by cesarean
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient's consent to participate in the study No history for diabetes, high blood pressure, heart disease Patients who have failed spinal anesthesia and undergo general anesthesia
Exclusion criteria
Exclusion criteria: Patients with contraindications of spinal anesthesia (ICP increase, shock, history of coagulation problems ..)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality motor block. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: Bromage scure.;Sensory block quality. Timepoint: 5-10-15 and30 minutes after analgesia. Method of measurement: visual analgesic scale.;Headache. Timepoint: A week after surgery. Method of measurement: visual analgesic scale. | — |
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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Hamedan University of Medical Sciences