跳至主要内容
临床试验/NL-OMON30792
NL-OMON30792尚未招募不适用

Prospective study into submicroscopic chromosomal abnormalities in foetuses with structural malformations on ultrasound - Submicroscopic chromosomal abnormalities and fetal malformations

Academisch Medisch Centrum0 个研究点目标入组 130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
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

  • Only if amniocentesis is already planned because of abnormal ultrasonographic findings of the fetus, future parents will be asked for this study.
  • The MLPA-test will only be performed if the karyotyping is normal.

排除标准

  • Abnormal fetal karyotype that can explain the ultrasonographic anomalies.
  • Absence of a signed informed consent by both parents.

研究者

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