NCT00840710Unknown不适用
Clinical Feasibility of Birth- Track II System
Barnev Ltd1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2010年2月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 15
- 试验地点
- 1
研究概览
简要总结
The Study purpose is to monitor the cervix dilation, head descent, FHR and to follow contraction in a women in active labor.
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
- 17 Years 至 50 Years（Child, Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Laboring women referred to the Maternity Center in active labor (3cm dilatation and contractions).
- •Gestational age 37-42 weeks. (GA)
- •Single fetus
- •Subjects who understood, agreed and signed the informed consent form
排除标准
- •Women with abnormal placentation (placenta previa)
- •Abnormal fetal presentation (breech presentation)
- •Maternal History of HIV and/or blood transmitted hepatitis and/or active genital Herpes.
- •Need for immediate delivery (cord prolapsed or suspected placental abruption)
研究者
研究点 (1)
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