Clinical Trials Directory

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UnknownNCT05396378

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

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

Status
Unknown
Phase
Study type
Observational
Enrollment
150 (estimated)
Sponsor
Women's Hospital HUS · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers

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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOral glucose in liquid formA glucose containing drink that has a fixed dose of 25 g of glucose per can.

Timeline

Start date
2023-07-01
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2022-05-31
Last updated
2023-04-25

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT05396378. Inclusion in this directory is not an endorsement.