Trials / Completed
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
| Type | Name | Description |
|---|---|---|
| DRUG | Norepinephrine | 0.05ug/kg/min Norepinephrine during Cesarean Section Operation |
| DRUG | Phenylephrine | 0.25ug/kg/min phenylephrine during Cesarean Section Operation |
| DRUG | Ringer's Solution | 3 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.