DRKS00025163已完成不适用
Clinical utility of rapid genome sequencing in critically ill children in Germany - Baby Lion
Institut für Humangenetik0 个研究点目标入组 130 人开始时间: 2023年2月6日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 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
- one 至 14 Years（—）
- 性别
- All
入选标准
- •Critically ill child on NICU or PICU with suspected genetic disorder (e.g. complex disease presentation involving two or more organ systems, unusually severe disease manifestation requiring intensive care, other family members with similar symptoms, extremely dystrophic newborns)
排除标准
- •Obvious non-genetic causes such as trauma
研究者
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