NL-OMON48381招募中不适用
PRegnancy Outcomes and Maternal Insulin Sensitivity - PROMIS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 130
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Healthy singleton pregnant women (10-12 weeks of gestation)
- •- BMI *25 kg/m2
- •- Fasting Blood Glucose (FBG *7.0 mmol/l)
- •- Dutch or English speaking
- •- Written informed consent
排除标准
- •- Serious health complications (Hypertension, Hyperlipidemia, Asthma, Haemochromatosis) or medication use that influence the glucose metabolism or fetal growth (e.g. corticosteroids).
- •- Multiple pregnancy
- •- pre-existing Diabetes type 1 and 2 defined as FBG *7.0 mmol/l or use of diabetes medication
- •- Participation in any other studies involving the investigation of medication or nutritional products or antibiotic use in the two weeks prior to entry into the study
- •- HIV/Hepatitis
- •- Expectation of non-compliance to the study protocol, among others, a fear of needles
- •- Known allergies or intolerances for nutritional ingredients in the MTT
- •- Psychological dysfunctions
研究者
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