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Coload Optimization Guided by Inferior Vena Cava Collapsibility Index

Not Applicable
Completed
Conditions
Adverse Effect
Interventions
Drug: 4 ml/kg group
Drug: 8 ml/kg group
Drug: 12 ml/kg group
Registration Number
NCT04272632
Lead Sponsor
General Hospital of Ningxia Medical University
Brief Summary

The purpose of this study is to investigate the optimal coload guided by inferior vena cava collapsibility index in parturients with prophylactic norepinephrine infusion undergoing cesarean section.

Detailed Description

Post-spinal anesthesia hypotension is a frequent complication during spinal anesthesia for cesarean section. The incidence of post-spinal anesthesia hypotension is as high as 62.1-89.7% if prophylactic measures are not taken. Vasopressors has been highly recommended for routine prevention and/or treatment of post-spinal anesthesia hypotension. As a potential substitute drug for phenylephrine, norepinephrine has gradually been used in parturients undergoing cesarean section. There's some evidence that prophylactic infusion of norepinephrine could effectively reduce the incidence of post-spinal anesthesia hypotension in parturients undergoing cesarean section. However, our study (NCT03997500) had been shown that inferior vena cava collapsibility index (IVC-CI) markedly decreased in prophylactic norepinephrine infusion versus normal saline after spinal anesthesia and fetal delivery, suggesting that more prudent fluid management is required. The ideal dose of coload and coload is still unknown. Thus, the purpose of this study is to investigate the optimal coload guided by IVC-CI in parturients with prophylactic norepinephrine infusion undergoing cesarean section.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
168
Inclusion Criteria
  • 18-40 years
  • Primipara or multipara
  • Singleton pregnancy ≥37 weeks
  • American Society of Anesthesiologists physical status classification I to II
  • Scheduled for elective cesarean section under spinal anesthesia
Exclusion Criteria
  • Body height < 150 cm
  • Body weight > 100 kg or body mass index (BMI) ≥ 40 kg/m2
  • Eclampsia or chronic hypertension or baseline blood pressure ≥ 160mmHg
  • Hemoglobin < 7g/dl
  • Fetal distress, or known fetal developmental anomaly

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
4 ml/kg group4 ml/kg group4 ml/kg compound sodium chloride (0.85% NaCl, 0.03% KCl, and 0.033% CaCl2) was given immediately after spinal anesthesia.
8 ml/kg group8 ml/kg group8 ml/kg compound sodium chloride (0.85% NaCl, 0.03% KCl, and 0.033% CaCl2) was given immediately after spinal anesthesia.
12 ml/kg group12 ml/kg group12 ml/kg compound sodium chloride (0.85% NaCl, 0.03% KCl, and 0.033% CaCl2) was given immediately after spinal anesthesia.
Primary Outcome Measures
NameTimeMethod
The minimum (IVC-min), maximum diameter (IVC-max) and collapsibility index (IVC-CI) of the inferior vena cava (IVC)Before leaving the operating room

IVC-CI = \[(IVC-max-IVC-min) /IVC-max\*100%\]

Secondary Outcome Measures
NameTimeMethod
APGAR score5min after delivery

A= Appearance P=Pulse G=Grimace A=Attitude R=Respiration

Base excessImmediately after delivery

From umbilical vein blood gases

pHImmediately after delivery

From umbilical vein blood gases

Partial pressure of oxygenImmediately after delivery

From umbilical vein blood gases

The incidence of post-spinal anesthesia hypotension.1-15 minutes after spinal anesthesia

Systolic blood pressure (SBP) \< 80% of the baseline.

The incidence of severe post-spinal anesthesia hypotension.1-15 minutes after spinal anesthesia

Systolic blood pressure (SBP) \< 60% of the baseline

The incidence of nausea and vomiting.1-15 minutes after spinal anesthesia

Presence of nausea and vomiting in patients after spinal anesthesia

The incidence of bradycardia1-15 minutes after spinal anesthesia

Heart rate \< 55 beats/min.

The incidence of hypertension1-15 minutes after spinal anesthesia

Systolic blood pressure (SBP) \>120% of the baseline

Overall stability of systolic blood pressure control versus baseline1-15 minutes after spinal anesthesia.

Evaluated by performance error (PE).

Overall stability of heart rate control versus baseline1-15 minutes after spinal anesthesia.

Evaluated by performance error (PE).

Trial Locations

Locations (1)

General Hospital of Ningxia Medical University

🇨🇳

Yinchuan, Ningxia, China

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