NL-OMON31988尚未招募不适用
Sex chromosome abnormality as co-finding when performing routine prenatal diagnostic procedures: diagnostic gain or damage? Study on the views of parents and professionals. - Routine fetal gender determination in prenatal testing: gain or damage?
niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 30 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
- 发起方
- 入组人数
- 30
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
- •Parents that have undergone an invasive prenatal diagnostic test in the last 15 years in the Nijmegen region because of maternal age or to exclude other serious chromosomal anomalies, who were faced with a fetal sex chromosomal abnormality as a co-finding in the karyotyping procedure.
排除标准
- •. Patients with a clear risk at a sex chromosomal abnormality, because of an earlier child with this same problem.
- •. Patients with insufficient fluency in Dutch.
研究者
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