Hypotension. Hypotension
Conditions
Interventions
Intervention 1: Intervention group: patients in the intervention group received 100 micrograms per hour of Phenylephrine infusion. Intervention 2: Control group: patients in the control group received
Sponsors
Oroumia University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Pregnant women candidates for cesarean section under spinal anesthesia American Society of Anesthesiologists classification system I and II (ASA II and ASA II)
Exclusion criteria
Exclusion criteria: Patients with classical hypertension Gestational hypertension Patients with pulmonary and cardiovascular diseases Patients with cerebrovascular disease Fetal abnormality
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hypotension, which was considered as a decrease in systolic blood pressure by 80% of the baseline. Timepoint: Before the intervention and in 5, 15, 25, 35 and 45 minutes after the intervention. Method of measurement: Blood pressure monitoring device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hypertension was considered as an increase in systolic blood pressure above 120% of the baseline. Timepoint: Before the intervention and in 5, 15, 25, 35 and 45 minutes after the intervention. Method of measurement: Blood pressure monitoring device.;Nausea. Timepoint: Before the intervention and in 5, 15, 25, 35 and 45 minutes after the intervention. Method of measurement: Interview.;Vomiting. Timepoint: Before the intervention and in 5, 15, 25, 35 and 45 minutes after the intervention. Method of measurement: Interview.;Bradycardia (decrease in heart rate to less than 60 beats per minute). Timepoint: Before the intervention and in 5, 15, 25, 35 and 45 minutes after the intervention. Method of measurement: Heart rate monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Hadi Hooshyar
Oroumia University of Medical Sciences
Outcome results
None listed