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Glucose Monitoring Device Tested in Pregnant Women After Gastric Bypass

Compares a glucose sensor with finger-prick checks in pregnant women with diabetes after gastric bypass.

Plain-language title generated from the registry record
Registry title: Gestational Diabetes After Gastric Bypass Surgery

Key facts

Where
Lund, SwedenSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 50 years old?

Source: NCT06291766, who can take part

Where in Sweden

  • Region SkaneLund, SwedenTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Region Skane
Trial code
NCT06291766
Record updated
22 August 2025
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: 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: Other kinds of bariatric surgery.

ClinicalTrials.gov NCT06291766