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临床试验/NCT00069576
NCT00069576已完成不适用

A Randomized Clinical Trial of Treatment for Mild Gestational Diabetes Mellitus

The George Washington University Biostatistics Center31 个研究点 分布在 1 个国家目标入组 7,381 人开始时间: 2002年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
7,381
试验地点
31
主要终点
Number of Participants With Composite Neonatal Morbidity

研究概览

简要总结

Gestational diabetes mellitus (GDM) is a type of diabetes (high blood sugar) that occurs in pregnant women. This study will determine whether treating pregnant women who have mild GDM improves the health of their babies. The follow-up study will examine whether factors during the previous pregnancy (such as blood sugar during pregnancy) are associated with the woman and her child's health 4-9 years later.

详细描述

Gestational diabetes mellitus is defined as glucose intolerance of variable severity with onset or first recognition during pregnancy. The definition applies regardless of insulin use for treatment or the persistence of the condition after pregnancy, and does not exclude the possibility that unrecognized glucose intolerance or overt diabetes may have preceded the pregnancy. Pre-existing diabetes substantially contributes to perinatal morbidity and mortality. The association of milder forms of gestational diabetes with adverse pregnancy outcomes, including morbidities such as macrosomia, birth trauma, and neonatal hypoglycemia, remains questionable. While it is likely that maternal glucose intolerances reflect a continuum of risk for adverse outcomes, it is not known whether there is a benefit to identification and subsequent treatment of mild glucose intolerance during pregnancy. This study will determine whether dietary treatment (and insulin as required) for mild GDM will reduce the frequency of neonatal morbidity associated with mild glucose intolerance.

Participants in this study will receive a 50-gram glucose loading test (GLT) between 24 and 30 weeks' gestation. Those with a positive GLT will receive a subsequent 3-hour oral glucose tolerance test (OGTT). Based upon these test results, women will be assigned to 4 groups. Women with a positive GLT and abnormal OGTT will be randomly assigned to receive either nutritional counseling and diet therapy (Group 1) or no specific treatment (Group 2a). Women with a positive GLT but normal OGTT will be enrolled in Group 2b for observation. Women with a negative GLT will be enrolled in Group 3 and will serve as a control group.

Women in Group 1 will receive formal nutritional counseling and will be instructed on the techniques of self blood glucose monitoring. Patients will take daily blood glucose measurements and will be seen at weekly study visits. The study will evaluate birth outcomes, including stillbirth, neonatal hypoglycemia, neonatal hyperinsulinemia, neonatal hyperbilirubinemia, and birth trauma.

The follow-up study will examine if blood sugar levels and treatments during pregnancy influence the health of the mother and child several years later. The study will also examine whether there is a genetic link to the health of the mother and child. The study visit will include blood pressure, body size measurements, blood draw and saliva collection, and questions related to the mother and child's health and environment.

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
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Gestational age at enrollment 24 - 31 weeks

排除标准

  • Diabetes diagnosed prior to pregnancy
  • Abnormal gestational diabetes (>= 135 mg/dl) testing prior to 24 weeks' gestation
  • Gestational diabetes in a previous pregnancy
  • History of stillbirth or fetal death
  • Pregnancy with more than one fetus
  • Known major fetal anomaly
  • Current or planned corticosteroid therapy
  • Asthma requiring medication
  • Current or planned beta adrenergic therapy
  • Chronic hypertension requiring medication within 6 months of or during pregnancy
  • Chronic medical conditions such as HIV/AIDS, kidney disease, or congenital heart disease
  • Hematologic or autoimmune disease such as sickle cell disease, other hemoglobinopathies, lupus, or antiphospholipid syndrome
  • Maternal or fetal conditions likely to require preterm delivery, such as pre-eclampsia, preterm labor, or intrauterine growth retardation
  • Previous or planned tocolytic therapy to induce labor or increase contraction strength

研究组 & 干预措施

Nutritional counseling & self blood glucose monitoring

Active Comparator

Within one week of enrollment, women in the treatment group receive formal nutritional counseling and will be instructed on the technique of self blood glucose monitoring using a memory-based reflectance meter.

干预措施: nutritional counseling (Behavioral)

Nutritional counseling & self blood glucose monitoring

Active Comparator

Within one week of enrollment, women in the treatment group receive formal nutritional counseling and will be instructed on the technique of self blood glucose monitoring using a memory-based reflectance meter.

干预措施: self blood glucose monitoring (Behavioral)

No treatment

No Intervention

This group will not receive any specific dietary therapy except for written information concerning general nutritional recommendations for normal pregnancy.

结局指标

主要结局

Number of Participants With Composite Neonatal Morbidity

时间窗: Delivery through discharge of infant from hospital up to 120 days

The composite perinatal outcome included stillbirth, neonatal death, hypoglycemia, hyperbilirubinemia, elevated cordblood C-peptide level, and birth trauma.

Number of Children at the 5-10 Year Followup With BMI ≥ 95th Percentile for Age and Sex

时间窗: Age 5-10 years

Number of children with BMI ≥ 95th percentile for age and sex. BMI is measured as kg / m\^2. Standards based on the 2000 Centers for Disease Control growth charts.

次要结局

  • Mean Neonatal Birth Weight(Assessed at delivery)
  • Number of Neonates With Macrosomia (Birth Weight > 4000 gm)(Assessed at Delivery)
  • Mean Neonatal Fat Mass at Delivery(Assessed at delivery)
  • Number of Neonates Who Received Intravenous Glucose Treatment(Delivery through hospital discharge up to 120 days)
  • Number of Neonates Who Experienced Respiratory Distress Syndrome(Delivery through hospital discharge up to 120 days)
  • Number of Infants Admitted to NICU(Delivery through hospital discharge up to 120 days)
  • Number of Neonates Who Were Large for Gestational Age at Delivery(From time of randomization through delivery (up to 17 weeks))
  • Number Participants Who Delivered Preterm(Delivery before 37 weeks gestation)
  • Number of Neonates Who Were Small for Gestational Age(From time of randomization through delivery (up to 17 weeks))
  • Number of Participants Who Underwent Labor Induction(From time of randomization through induction (up to 17 weeks))
  • Number of Participants Who Underwent Cesarean Delivery(Delivery)
  • Number of Participants Who Experienced Preeclampsia(From time of randomization through delivery (up to 17 weeks))
  • Number of Neonates Who Experienced Shoulder Dystocia(During the process of labor through delivery)
  • Number of Participants Who Had Preeclampsia or Gestational Hypertension(From time of randomization through delivery (up to 17 weeks))
  • Mean Maternal Body-mass Index at Delivery(Delivery)
  • Number of Children at 5-10 Year Follow up With Waist Circumference >90th Percentile for Age, Sex and Race/Ethnicity(Age 5-10 years)
  • Number of Children at 5-10 Year Follow up With Hypertension ≥ 95th Percentile for Age, Sex and Height(Age 5 - 10 years)
  • Mean Maternal Weight Gain(From time of randomization through delivery (up to 17 weeks))
  • Number of Children With BMI ≥ 85th Percentile for Age and Sex(Age 5-10 years)
  • Number of Children at 5-10 Year Follow-up With Impaired Fasting Glucose ≥100 mg/dL(Age 5-10 years)

研究者

发起方
The George Washington University Biostatistics Center
申办方类型
Other
责任方
Sponsor

研究点 (31)

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