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Gestational Diabetes After Gastric Bypass Surgery

NCT06291766 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2025-08-22

No results posted yet for this study

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.

Conditions

  • Diabetes, Gestational
  • Gastric Bypass Status for Obesity Complicating Pregnancy, Childbirth, or the Puerperium
  • Pregnancy in Diabetic
  • Blood Glucose Self Monitoring

Interventions

DEVICE

FreeStyle 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

Sponsors & Collaborators

  • Region Skane

    lead OTHER

Principal Investigators

  • Ulrika Moll, MD, PhD · Region Skane

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2028-12-31
Completion
2035-12-31
FDA Device
Yes

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06291766 on ClinicalTrials.gov