Early Recovery After Cesarean Delivery - Maternal Glucose Homeostasis Following Preoperative Glucose Dose
- Conditions
- Cesarean Section ComplicationsGestational Diabetes
- Registration Number
- NCT05396378
- Lead Sponsor
- Women's Hospital HUS
- Brief 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.
- Detailed 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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Female
- Target Recruitment
- 150
- Volunteers to participate in the study
- Diabetes, either gestational or type II
- Planned for cesarean delivery
- Type I diabetes
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase of blood glucose following the oral glucose dose 4 hours The effect of oral glucose dose on the parturient's blood glucose level (mM)
- Secondary Outcome Measures
Name Time Method Maternal subjective well being after oral glucose dose during the preoperative fasting period 4 hours subjective assessment by the parturient (categorial)
Trial Locations
- Locations (1)
HUS/Women's hospital dept of obstetrics
🇫🇮Helsinki, Finland
HUS/Women's hospital dept of obstetrics🇫🇮Helsinki, Finland