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临床试验/NCT03029702
NCT03029702已完成4 期

Metabolic Analysis for Treatment Choice in Gestational Diabetes Mellitus

Maisa N. Feghali, MD1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2018年2月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
54
试验地点
1
主要终点
Proportion of Women Who Are Eligible, Screened, Enroll and Remain in the Study

研究概览

简要总结

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).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Study team members assessing delivery outcomes will be masked to the participant's study assignment

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

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

排除标准

  • 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

研究组 & 干预措施

Usual Care

Active Comparator

Participants will undergo standard counseling and be prescribed a treatment for their GDM. Treatments include insulin, glyburide, and metformin.

干预措施: Insulin (Drug)

Usual Care

Active Comparator

Participants will undergo standard counseling and be prescribed a treatment for their GDM. Treatments include insulin, glyburide, and metformin.

干预措施: Glyburide (Drug)

Usual Care

Active Comparator

Participants will undergo standard counseling and be prescribed a treatment for their GDM. Treatments include insulin, glyburide, and metformin.

干预措施: Metformin (Drug)

Individualized Treatment

Active Comparator

Participants will undergo standard counseling and be matched to therapy based on their GDM mechanism. Treatments include insulin, glyburide, and metformin.

干预措施: Insulin (Drug)

Individualized Treatment

Active Comparator

Participants will undergo standard counseling and be matched to therapy based on their GDM mechanism. Treatments include insulin, glyburide, and metformin.

干预措施: Glyburide (Drug)

Individualized Treatment

Active Comparator

Participants will undergo standard counseling and be matched to therapy based on their GDM mechanism. Treatments include insulin, glyburide, and metformin.

干预措施: Metformin (Drug)

结局指标

主要结局

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

时间窗: Through study completion, an average of 16 weeks

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

Proportion of Participants Who Report Suitability of the Study Procedures

时间窗: Through study completion, an average of 16 weeks

Suitability of the study procedures and interventions to participants assessed through one-on-one qualitative interview

次要结局

  • Proportion of Participants With Consistent GDM Mechanism Before and and After Treatment Initiation(2 weeks after treatment initiation)
  • Proportion of Women Who Remain on Same Treatment During Study(Through study completion, an average of 16 weeks)
  • Maternal Glucose Control(Delivery)
  • Proportion of Participants Who Deliver by Primary Cesarean(Delivery)
  • Proportion of Participants Who Developed Hypertensive Diseases in Pregnancy(Delivery)
  • Birthweight(Delivery)
  • Neonatal Lean Body Mass(Within 72 hours of delivery)
  • Cord Blood Glucose(Delivery)
  • Cord Blood C-peptide(Delivery)

研究者

发起方
Maisa N. Feghali, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Maisa N. Feghali, MD

Assistant Professor

University of Pittsburgh

研究点 (1)

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