Effect of norepinephrine with phenylephrine in the prevention of hypotension undergoing spinal anesthesia
Phase 3
- Conditions
- Hypotension.Hypotension
- Registration Number
- IRCT20201207049639N8
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
Satisfaction to participate in the study
Age between 20 to 45 years
Lack of sensitivity to norepinephrine and phenylephrine
Exclusion Criteria
Having liver, kidney and heart disease
Sensitivity to anesthetics
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Systolic blood pressure. Timepoint: Before intervention, 5, 10, 15, 20, 25 and 30 minutes after intervention. Method of measurement: Blood pressure monitor.;Diastolic blood pressure. Timepoint: Before intervention, 5, 10, 15, 20, 25 and 30 minutes after intervention. Method of measurement: Blood pressure monitor.
- Secondary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: It is recorded up to 30 minutes after the intervention if observed. Method of measurement: Observation.