Cesarean Section Clinical Trial
Official title:
The Effect of Administering a Small Dose of Glucose on the Pregnant Women and Their Neonates During Cesarean Section
The purpose of this study is to investigate the effect of administering a small dose of glucose on the pregnant women and their neonates during cesarean section. We investigate the safety and efficacy of use of a glucose-containing solution for the pregnant women and the neonates.
Rapid infusion of large amount of glucose is associated with fetal hyperglycemia,
hyperinsulinemia, and neonatal hypoglycemia. However, the effect of small dose of glucose is
unclear. We conducted a pilot study of small dose of glucose. We investigated the effect of
a glucose-containing fluid on the blood sugar of the umbilical artery. We found that in the
case of no-glucose-containing fluid, there were some cases in which umbilical arterial
concentration of glucose was less than 50 mg/dl, which might cause neonatal hypoglycemia. In
addition, in the case of 1%-glucose-containing fluid, mean umbilical arterial concentration
of glucose was 97 mg/dl.
The purpose of this study is to investigate the effect of administering a small dose of
glucose on the pregnant women and their neonates during cesarean section. We investigate the
safety and efficacy of use of a glucose-containing solution for the pregnant women and the
neonates.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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