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CompletedNCT03833895

The Phenylephrine vs. Norepinephrine Infusion Undergoing Cesarean Section

The Phenylephrine vs. Norepinephrine Infusion by Lidico Monitoring With Pregnancy Patients Undergoing Cesarean Section

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
238 (actual)
Sponsor
China International Neuroscience Institution · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Compare 0.05 μg/kg/min Norepinephrine and 0.25 μg/kg/min phenylephrine effect on fetus and parturient during Cesarean Section

Detailed description

1. Compare 0.05 μg/kg/min Norepinephrine and 0.25 μg/kg/min phenylephrine and control group effect on parturient hemodynamic change (systolic blood pressure SBP, diastolic blood pressure DBP,mean arterial pressure MAP,heart rate HR) and on LIDICO-rapid monitoring ( stroke volume SV, systemic vascular resistance SVR, cardiac output CO) and peripheral vein (PV) blood gas during Cesarean Section. 2. Compare 0.05 μg/kg/min Norepinephrine and 0.25 μg/kg/min phenylephrine and control group effect on fetus by blood gas of the umbilical vein (UV), umbilical artery (UA),

Conditions

Interventions

TypeNameDescription
DRUGNorepinephrine0.05ug/kg/min Norepinephrine during Cesarean Section Operation
DRUGPhenylephrine0.25ug/kg/min phenylephrine during Cesarean Section Operation
DRUGRinger's Solution3 ml/kg/min of LR was administrated according to standard weight.

Timeline

Start date
2019-02-20
Primary completion
2019-09-01
Completion
2019-09-02
First posted
2019-02-07
Last updated
2020-02-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03833895. Inclusion in this directory is not an endorsement.