NCT06291766Recruiting
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.
Source: ClinicalTrials.gov · Last updated 22 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- First submitted
- 5 Feb 2024
- Start date
- 1 Jan 2024
- Primary completion date
- Dec 2028
- Lead sponsor
- Region Skane
- Diseases
- Obesity
- NCT number
- NCT06291766
What you commit to
- Study type: Interventional
- Planned participants: 120
- From 1 Jan 2024 to the primary completion date, Dec 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Other kinds of bariatric surgery
Who the study is looking for
- 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
Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Region Skane Coordinator of this site? Confirm its status | Lund | Sweden | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.