ISRCTN52590306进行中（未招募）未知
Rapid genomic sequencing for the diagnosis of critically ill children in the NHS Genomic Medicine Service: A mixed-methods evaluation to ensure an equitable and effective parent and patient-centred service
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 入组人数
- 230
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
- 性别
- All
入选标准
- •1. Parents/carers of children with rare or undiagnosed conditions
- •2. Parents who have been offered rapid genomic sequencing because their baby or child was critically ill
- •3. Parents who have been offered rapid genomic sequencing to inform management of a current pregnancy because they had a previously affected undiagnosed fetus/child
- •4. Professionals from clinical genetics and paediatrics specialties
- •5. Over 18 years of age
- •6. Able to give consent for participation
排除标准
- •Under 18 years of age
研究者
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