The Impact of Continous Glucose Monitoring on Pregnancy Outcome, in Women With Gestational Diabetes and a History of Gastric Bypass Surgery.

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this trial is to compare different means of glucose monitoring in women with gestational diabetes and a history of gastric bypass surgery. The main question it aims to answer is: How does continous glucose monitoring impact the treatment and affect pregnancy outcome in these women. Participants will be randomized to either continous glucose monitoring or regular capillary glucose measurements during the last trimester of their pregnancy. Researchers will compare the glucose measurement outcomes, the glucose lowering treatment given and pregnancy outcomes between groups.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: f
View:

• Understands written and spoken Swedish

• Previous Gastric Bypass surgery

• Diagnosed with gestational diabetes according to our local criteria

• Planned follow up at the Specialized Maternity Ward at Skane University Hospital

• Understands the use of CGM and is willing to use the system

• Have signed informed consent

Locations
Other Locations
Sweden
Region Skane
RECRUITING
Lund
Contact Information
Primary
Ulrika Moll, MD, PhD
ulrika.moll@skane.se
+46733307170
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2035-12
Participants
Target number of participants: 120
Treatments
Other: Continous glucose measurement
Use of FreeStyle Libre 3, with Libre Link app and Glooko app for measurement and review of glucose measurements.
No_intervention: Capillary glucose measurement
Standard care, including capillary glucose measurements and Glooko app for review of glucose measurements.
Sponsors
Leads: Region Skane

This content was sourced from clinicaltrials.gov