Evaluation of the Phenylephrine effect on hypotension in cesarean sectio
Phase 3
- Conditions
- Hypotension.Hypotension
- Registration Number
- IRCT20201207049639N1
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
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
Patients with classical hypertension
Gestational hypertension
Patients with pulmonary and cardiovascular diseases
Patients with cerebrovascular disease
Fetal abnormality
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.