Pilot Study of Continuous Glucose Monitoring for Postpartum Glucose Screening

This study is looking at a new way to screen for diabetes after pregnancy in women who had gestational diabetes (diabetes during pregnancy). Currently, a test called an Oral Glucose Tolerance Test (OGTT) is used, but many women find it difficult to complete. This study will offer a Continuous Glucose Monitor (CGM) called the Freestyle LibrePro by Abbott for 14 days as an alternative. We want to see if using CGM, which is a low-burden and remote way to check blood sugar, can encourage more women to get screened. You may be able to join if you are 12-16 weeks postpartum, had gestational diabetes in your most recent pregnancy, and have an OGTT ordered. The main goal is to see how many eligible patients choose to use the CGM for screening. This study is currently recruiting up to 1300 participants.

Study design
This is an interventional study that plans to enroll up to 1300 women. It is testing a new screening method against the current standard.
What's involved
You would use a Continuous Glucose Monitor (CGM) for 14 days. This would be done remotely.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint, Continuous Glucose Monitor (CGM) uptake, is measured at 20 weeks postpartum.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07332416

Pilot Study of Continuous Glucose Monitoring for Postpartum Glucose Screening

Enrolling by Invitation
NAAges 18+InterventionalScreening
Wake Forest University Health Sciences
~1,300 participants
Updated 2026-07-10 on ClinicalTrials.gov
What's tested:Continuous glucose monitoring for 14 days using the Freestyle LibrePro by Abbott

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Continuous Glucose Monitor (CGM) uptake - Percentage of CGM-eligible patients
Measured over 20 weeks postpartum
Gestational Diabetes
1 sites across 1 states
North Carolina1
  • Katherine A Sauder, MD · PRINCIPAL_INVESTIGATOR · Wake Forest University Health Sciences

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

12-16 weeks postpartum
Gestational diabetes Mellitus (GDM) diagnosis in most recent pregnancy
Oral Glucose Tolerance Test (OGTT) order placed in the medical record

Exclusion

Pre-gestational diabetes
Non-English language
  • Continuous Glucose Monitor (CGM) uptake - Percentage of CGM-eligible patients20 weeks postpartum

    Percentage of CGM-eligible patients that return a used CGM sensor