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NOT YET RECRUITING
NCT07034261
NA

Continuous Glucose Monitoring to Detect Postpartum Dysglycemia in Patients With Gestational Diabetes

Sponsor: University of Chicago

View on ClinicalTrials.gov

Summary

The aim of this study is to determine the ability of postpartum continuous glucose monitoring (CGM) for subjects with gestational diabetes (GDM) to predict dysglycemia on 4-12 week postpartum oral glucose tolerance test (OGTT).

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2026-04

Completion Date

2026-09

Last Updated

2026-02-13

Healthy Volunteers

No

Interventions

DEVICE

Blinded Continuous Glucose Monitoring Device

Subjects will be asked to wear blinded continuous glucose monitoring device for 14 days.