Magee Womens Hospital of UPMC
Pittsburgh, Pennsylvania, 15213, United States
NCT Number: NCT03029702
Gestational diabetes (GDM) is a significant clinical and public health burden, affecting over 400,000 pregnant women in the United States each year. Without adequate treatment, women with GDM and their infants are at risk for substantial morbidity. Because of this, experts recommend treatment focused on normalization of hyperglycemia to improve outcomes. However, providers have limited capacity to predict which treatment will achieve glycemic goals. This results in a choice based on provider and patient preference and a trial and error approach, which can create delays in glycemic control within the short (8-10 weeks) window between diagnosis and delivery. Maternal and fetal morbidity may be related to a mismatch between glycemic pathophysiology and the mechanism of action of glucose-lowering agents. In fact, GDM is heterogeneous, with predominant insulin resistance (IR) in 50%, insulin secretion deficit (ISD) in 30%, and a combination of both in 20% of women as underlying mechanisms of hyperglycemia. This variation in GDM pathophysiology and clinical outcomes supports the use of an individualized treatment approach. The overall goal of this project is to investigate an individualized treatment approach for GDM where treatment is based on each woman's GDM mechanism. The study will employ the same treatment in both arms, but choice of treatment will differ based on study arm (matched or unmatched to GDM mechanism).
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Notify Me18 year–45 year
Female
Interventional
Phase 4
Pittsburgh, Pennsylvania, 15213, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Insulin will be used for GDM treatment
Glyburide will be used for GDM treatment
Metformin will be used for GDM treatment
Time frame: Through study completion, an average of 16 weeks
Proportion of women who are eligible, screened, enrolled and remain in the study
Time frame: Through study completion, an average of 16 weeks
Suitability of the study procedures and interventions to participants assessed through one-on-one qualitative interview
Time frame: 2 weeks after treatment initiation
Time frame: Through study completion, an average of 16 weeks
Time frame: Delivery
>50% fasting below 95 and 1 hour postprandial < 140 during the 4 weeks before delivery
Time frame: Delivery
Time frame: Delivery
Time frame: Delivery
Time frame: Within 72 hours of delivery
Time frame: Delivery
Time frame: Delivery
Maisa N. Feghali, MD
Other
Acronym: MATCh-GDM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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