NL-OMON47377招募中不适用
Genetic Origin of Congenital Heart Disease Identification of genetic variants causing congenital heart disease - GO Heart study
niversitair Medisch Centrum Utrecht0 个研究点目标入组 1,050 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
- 招募中
- 发起方
- 入组人数
- 1,050
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
- 2 至 99（—）
入选标准
- •- Patient has Congenital Heart Disease
- •- Patient undergoes an invasive procedure (cardiac catheterization or cardiac surgery) during which DNA can be obtained
排除标准
- •(1) No informed consent obtained for present study.
- •(2) Patients that do not allow to be informed about unexpected genotypic findings to which known treatments are available.
- •(3) No informed consent for blood sample drawing by one of the parents for NGS
- •(4) Patient is a monozygotic twin.
研究者
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