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RECRUITING
NCT06184373

Early Investigation of Glucose Monitoring After Gestational Diabetes Pilot

Sponsor: Ohio State University

View on ClinicalTrials.gov

Summary

One third of women with gestational diabetes (GDM), diabetes diagnosed during pregnancy, have abnormal glucose levels within 3 years after pregnancy, but follow up is low. Continuous glucose monitors (CGM), a small sensor inserted under the skin, may be able to screen women with GDM for diabetes risk. The investigators will ask postpartum women to use CGM at 6-8 weeks postpartum and answer surveys about quality of life after wearing the CGM. The investigators will collect data on blood glucose trends for future studies if participants find CGM use acceptable. The investigators hope to learn if CGM could improve postpartum follow up experiences for people with recent GDM.

Official title: Early Investigation of Glucose Monitoring After Gestational Diabetes (ENGAGED): Utility and Acceptability of Continuous Glucose Monitoring in the Early Postpartum Period After Gestational Diabetes Mellitus

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

OBSERVATIONAL

Enrollment

20

Start Date

2025-06-06

Completion Date

2027-05-30

Last Updated

2026-01-22

Healthy Volunteers

Yes

Interventions

DEVICE

Continuous glucose monitor

CGMs will be worn for a maximum of 10 days at 6-8 weeks postpartum.

DIAGNOSTIC_TEST

Oral Glucose Tolerance Test

At 10-12 weeks postpartum, participants will complete an oral glucose tolerance test, which involves drinking a glucose substance and having glucose levels measured a maximum of 3 times.

DIAGNOSTIC_TEST

Hemoglobin A1c

At 11-14 months postpartum, participants will be asked to have their blood drawn to check their hemoglobin A1c to look for signs of developed insulin resistance

Locations (1)

Ohio State University Medical Center

Columbus, Ohio, United States