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The effect of phenylephrine on blood pressure and nausea and vomiting in pregnant wome

Phase 3
Conditions
Pregnancy.
Pre-existing hypertension complicating pregnancy, childbirth and the puerperium
Registration Number
IRCT20191007045023N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

Pregnant women 18-45 years
Pregnant women candidates for cesarean section by spinal anesthesia
ASA Class 1 and 2
Elective cesarean section

Exclusion Criteria

history of allergy to phenylephrine
BMI>30 Kg/M2
hypertension (>140/90 mmHg)
contraindication for spinal anesthesia
severe cardiovascular disease
prematurity
emergency cesarean section
inadequate analgesia after spinal anesthesia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Systolic blood pressure. Timepoint: every two minutes. Method of measurement: sphygmomanometer.;Diastolic blood pressure. Timepoint: every two minutes. Method of measurement: sphygmomanometer.;Heart rate. Timepoint: every two minutes. Method of measurement: puls oxymetrie.
Secondary Outcome Measures
NameTimeMethod
Arterial pressure. Timepoint: Every two minutes. Method of measurement: Sphygmomanometer.;SPO2. Timepoint: Every two minutes. Method of measurement: Pulse oximetry.;Nausea. Timepoint: One time, imminently after delivery. Method of measurement: Observing.;PH. Timepoint: One time, imminently after delivery. Method of measurement: Blood sample.;PCO2. Timepoint: One time, imminently after delivery. Method of measurement: Blood sample.;HCO3. Timepoint: One time, imminently after delivery. Method of measurement: Blood sample.;Apgar 1. Timepoint: One time, imminently after delivery. Method of measurement: Observing.;Apgar 5. Timepoint: One time, imminently after delivery. Method of measurement: Observing.
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