Actively Recruiting
Preventing T2DM After GDM With Immediate Postpartum Screening
Led by University of Massachusetts, Worcester · Updated on 2025-07-18
116
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The overall goal of this proposal is to create and test an implementation protocol for in-hospital immediate postpartum diabetes screening for postpartum patients with pregnancies affected by GDM.
CONDITIONS
Official Title
Preventing T2DM After GDM With Immediate Postpartum Screening
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnancy complicated by gestational diabetes diagnosed with traditional two step testing in the third trimester according to Carpenter-Coustan Criteria
- Receiving prenatal care at UMASS Memorial and plans to deliver at UMASS Memorial
- Able and willing to provide informed consent
- Ability to complete immediate in hospital postpartum glucose testing
- Evidence of impaired glucose metabolism defined as fasting glucose value of 6126 mg/dL or 2-hour glucose value of 6200 mg/dL
You will not qualify if you...
- Known diagnosis of pre-existing pre-gestational diabetes in pregnancy
- Inability to complete oral glucose tolerance test (e.g., gastric bypass surgery history, gastric dumping syndrome history, vomiting of oral glucose tolerance test) in pregnancy or immediately postpartum
- Systemic steroid use
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Massachusetts Memorial Medical Center
Worcester, Massachusetts, United States, 01605
Actively Recruiting
Research Team
G
Gianna Wilkie, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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