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NCT Number: NCT03029702

Metabolic Analysis for Treatment Choice in Gestational Diabetes Mellitus

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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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women beyond 24 weeks of gestation who are scheduled for a 3-hour oral glucose tolerance test.

Exclusion criteria

  • Fetal anomaly
  • Pregestational diabetes
  • GDM diagnosis without a 3-hour OGTT
  • Multifetal gestation
  • Treatment with non-inhaled steroids within 7 days
  • Allergy to glyburide, metformin or sulfa
  • History of severe pulmonary (pulmonary requirement for oxygen therapy or daily treatment for restrictive of obstructive pulmonary disease)
  • Hepatic (LFT's greater than two times of upper normal range)
  • Renal (serum creatinine higher than 1.2 mg/dL) disease
  • History of heart failure or myocardial infarction

Treatment and study plan

Insulin

Drug

Insulin will be used for GDM treatment

Glyburide

Drug

Glyburide will be used for GDM treatment

metformin

Drug

Metformin will be used for GDM treatment

Primary outcomes

  1. Proportion of Women Who Are Eligible, Screened, Enroll and Remain in the Study

    Time frame: Through study completion, an average of 16 weeks

    Proportion of women who are eligible, screened, enrolled and remain in the study

  2. Proportion of Participants Who Report Suitability of the Study Procedures

    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

Secondary outcomes

  1. Proportion of Participants With Consistent GDM Mechanism Before and and After Treatment Initiation

    Time frame: 2 weeks after treatment initiation

  2. Proportion of Women Who Remain on Same Treatment During Study

    Time frame: Through study completion, an average of 16 weeks

  3. Maternal Glucose Control

    Time frame: Delivery

    >50% fasting below 95 and 1 hour postprandial < 140 during the 4 weeks before delivery

  4. Proportion of Participants Who Deliver by Primary Cesarean

    Time frame: Delivery

  5. Proportion of Participants Who Developed Hypertensive Diseases in Pregnancy

    Time frame: Delivery

  6. Birthweight

    Time frame: Delivery

  7. Neonatal Lean Body Mass

    Time frame: Within 72 hours of delivery

  8. Cord Blood Glucose

    Time frame: Delivery

  9. Cord Blood C-peptide

    Time frame: Delivery

Sponsors and collaborators

Lead sponsor

Maisa N. Feghali, MD

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Registry information

Acronym: MATCh-GDM

Important dates

Study start
2018
Primary completion
2023
Study completion
2023
First posted
Jan 24, 2017
Registry last updated
Nov 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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