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临床试验/NCT00314691
NCT00314691终止不适用

Development of New Prenatal Diagnostic Tests From Maternal Blood

University Hospital, Strasbourg, France2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2006年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
10
试验地点
2
主要终点
Feasibility of fetal gender and genotype determination out of maternal blood

研究概览

简要总结

After extraction of the cell-free DNA circulating in maternal plasma, we aim at developing new techniques for fetal DNA enrichment to perform fetal gender determination, and indirect diagnosis of inherited diseases like Cystic Fibrosis, Huntington Disease, Myotonic Dystrophy, B-Thalassaemia...

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Mother and father-to-be both older than 18 years old
  • Mother and father-to-be affiliated to social security
  • Mother and father-to-be have good understanding of the protocol
  • Pregnancy of the mother-to-be attested

排除标准

  • Mother and father-to-be are younger than 18 years old
  • Mother and/or father-to be refusing to participate

结局指标

主要结局

Feasibility of fetal gender and genotype determination out of maternal blood

次要结局

未报告次要终点

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other

研究点 (2)

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