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临床试验/NCT01623934
NCT01623934进行中(未招募)不适用

Role of Adipokines in Glucose Regulation During Pregnancy and in Fetal Development

Université de Sherbrooke1 个研究点 分布在 1 个国家目标入组 1,034 人开始时间: 2010年1月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,034
试验地点
1
主要终点
Diagnosis of gestational diabetes mellitus

研究概览

简要总结

This study includes 2 phases. During phase 1, pregnant women are followed over the course of pregnancy. The phase 2 is a follow-up of the mother-child dyad at 3, 5 and 10-12 year after delivery.

The purpose of this phase 1 is to :

  • assess the contribution and interactions of adipokines in the development of insulin resistance during pregnancy and gestational diabetes;
  • assess levels of maternal adipokines as determinants of development and fetal growth;
  • determine the genetic variations that influence levels of adipokines and glucose regulation during pregnancy and in newborns.

The purpose of this phase 2 is to:

  • identify DNA methylation variations at birth that are predictive of childhood overweight/obesity.
  • identify maternal characteristics associated with DNA methylation variations predictive of childhood overweight/obesity.
  • establish whether the loci predictive of childhood overweight/obesity at birth are still differentially methylated at 5 years of age (samples collected at 5 years of age).
  • identify DNA methylation variations at birth that are predictive of childhood neurodevelopment problems at 3, 5 and 10 years of age.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • age ≥ 18 yrs
  • gestational age between 6 and 13 weeks from last menstrual period
  • no recognized diabetes or drugs interfering with glucose metabolism
  • alcohol < 2 drinks/day
  • not involved in regular high intensity physical activity
  • otherwise good health status

排除标准

  • twin pregnancy

结局指标

主要结局

Diagnosis of gestational diabetes mellitus

时间窗: 24-28 weeks of gestation

75g oral glucose tolerance test

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marie-France Hivert

Md, MMSc

Université de Sherbrooke

研究点 (1)

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