NCT01104454已完成不适用
Placenta and Cord Blood Analyses
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Placenta, cord blood and umbilical analyses
研究概览
简要总结
The purpose of this study is to standardize methods in collecting and processing placenta, umbilical cord and cord blood samples. Samples will be used to determine potential differences between normal weight, overweight and obese individuals.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •at least 7 months pregnant
- •18 years of age or older
排除标准
- •underweight (BMI<18.5)
结局指标
主要结局
Placenta, cord blood and umbilical analyses
时间窗: at delivery
次要结局
未报告次要终点
研究者
研究点 (1)
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