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Early Recovery After Cesarean Delivery - Maternal Glucose Homeostasis Following Preoperative Glucose Dose

Gestational Diabetes Clinical Trial

Official title:
Early Recovery After Cesarean Delivery - Maternal Glucose Homeostasis Following Preoperative Glucose Dose in Diabetic Parturients

Clinical Trial Summary

Diabetic parturients planned for cesarean delivery will be recruited for the study. They will receive a fixed glucose dose to mimize the effects of fasting preoperatively and their blood glucose levels will be monitored.

Clinical Trial Description

Informed voluntary parturients planned for cesarean delivery will be informed about the study. The parturients will get prepacked glucose drink containing 100 g and 50 g glucose, respectively. They will consume the 100 g of glucose the night before the planned operation and the 50 g on the morning of the planned cesarean delivery. Their blood glucose level will be monitored by percutaneous continuous blood glucose monitoring every 30 minutes for 2 hours following the glucose dose in the evening and for four hours in the morning of the operation. The subjective well being of these parturients will be also qualitatively assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05396378
Study type Observational
Source Women's Hospital HUS
Contact Marja Kaijomaa, MD PhD
Phone 358504279650
Email marja.kaijomaa@hus.fi
Status Not yet recruiting
Phase
Start date July 1, 2023
Completion date December 31, 2023
View Details
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