Gestational Diabetes After Gastric Bypass Surgery
Recruiting · NCT06291766 · Interventional (participants receive a specific treatment) · Lead sponsor: Region Skane
View the official record on ClinicalTrials.gov →Interventions studied
FreeStyle Libre 2, continous glucose monitoring
What this trial is about
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.
Who can take part
Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 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
Exclusion criteria
- Other kinds of bariatric surgery
Where it is running
1 location listed.
- Region Skane - Lund, Sweden