RecruitingNot ApplicableNCT06291766

Gestational Diabetes After Gastric Bypass Surgery

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


Sponsor

Region Skane

Enrollment

120 participants

Start Date

Jan 1, 2024

Study Type

INTERVENTIONAL

Conditions

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

Sex: FEMALEMin Age: 18 YearsMax Age: 50 Years

Inclusion Criteria6

  • 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 Criteria1

  • Other kinds of bariatric surgery

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Interventions

DEVICEFreeStyle Libre 2, continous glucose monitoring

The use of FreeStyle Libre 3 sensors and Libre Link app and Glooko app for analysing glucose control in pregnancy


Locations(1)

Region Skane

Lund, Sweden

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NCT06291766


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