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临床试验/NCT02893072
NCT02893072Unknown不适用

Individualized Medical Nutrition Therapy Intervention Program for Women With Gestational Diabetes

The Third Xiangya Hospital of Central South University1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2015年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
600
试验地点
1
主要终点
intravenous glucose

研究概览

简要总结

Gestational diabetes mellitus (GDM) is one of the most frequent complications of pregnancy, that affect between 1 to 14% of population around the world. The overall purpose of this study is to determine the efficacy of individualized medical nutrition therapy (MNT) intervention to reduce and control the development of GDM.

详细描述

The number of women with gestational diabetes mellitus had been increasing. Maternal GDM has a great impact on both the health of the mothers and the offspring. Antenatal lifestyle interventions, in particular dietary intervention appear to be feasible to improve maternal GDM and weight gain. To the best of our knowledge, there has been no such trial examining the feasibility of MNT intervention in pregnant women in Hu'nan province. The aim of this study is to evaluate the efficacy of individualized MNT intervention to reduce and control the development of GDM. This is a prospective study, 500 patients who meet inclusion and exclusion criteria will be included. The changes of glucose and weight will be evaluated every two weeks.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Women with gestational diabetes

排除标准

  • 未提供

研究组 & 干预措施

Individualized medical nutrition therapy

Experimental

A comparison of normal lifestyle and medical nutrition therapy after intervention in the same individual

干预措施: Individualized medical nutrition therapy (Behavioral)

结局指标

主要结局

intravenous glucose

时间窗: every two weeks, from date of randomization until the date of parturition, assessed up to 10 months

Investigators will measure the participants' intravenous glucose every two weeks.From date of randomization until the date of parturition,assessed up to 10 months.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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