跳至主要内容
临床试验/NCT01907425
NCT01907425终止不适用

Prenatal Molecular Characterisation by CGH+SNP-ARRAY of Supernumerary Marker Chromosomes and de Novo Apparently Balanced Reciprocal Translocations

Centre Hospitalier Universitaire Dijon2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2013年8月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
35
试验地点
2
主要终点
supernumerary chromosome markers

研究概览

简要总结

In the prenatal period, les supernumerary marker chromosomes (SMC) and de novo apparently balanced reciprocal translocations are revealed by foetal karyotyping, which does not always make it possible to determine whether the anomaly is balanced or not and does not reveal uniparental disomy. The presence of these chromosomal rearrangements raises a difficult question for genetic counselling during pregnancy because of the risk of intellectual deficiency in the foetus. CGH+SNP-Array can provide information concerning 1) the balanced or not nature of these translocations 2) the presence or not of euchromatin in the SMC 3) the presence or not of uniparental disomy.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Metaphase karyotyping with SMC or a de novo Apparently-balanced reciprocal translocation
  • Parents covered by the National Health Insurance Agency,
  • Consent of the parents

排除标准

  • Persons not covered by the National Health Insurance Agency
  • Normal foetal karyotyping or showing chromosomal anomalies not related to the present study (trisomy 18....) or inherited anomalies
  • Absence of a sample from one of the parents

研究组 & 干预措施

Pre-natal Patient

Other

干预措施: Blood samples (Other)

结局指标

主要结局

supernumerary chromosome markers

时间窗: baseline

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 (2)

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