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Clinical Trial Summary

The goal is to evaluate the glycemic and hemodynamic stability in patients undergoing caesarean section in patients treated with maltodextrins two hours before the cesarean section


Clinical Trial Description

The patients undergoing elective cesarean section will be randomly divided in two groups: patients who drink 200 ml of clear liquid two hours before surgery or patients treated with 200 ml maltodextrins two hours before the surgery. The glycemic control will be done immediately before the maldodextrin administration and after the cesarean section by gluco stick. Standard hemodynamic monitoring ECG, Heart Rate, Blood pressure, Temperature, preipheral oxygen saturation will be done routinely. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05553756
Study type Interventional
Source University of Foggia
Contact
Status Active, not recruiting
Phase N/A
Start date April 13, 2020
Completion date December 31, 2022

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