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临床试验/NL-OMON43233
NL-OMON43233已完成不适用

Personalised Risk assessment in Febrile illness to Optimise Real-life Management across the European Union (PERFORM) <br> - PERFORM

Radboud Universitair Medisch Centrum0 个研究点目标入组 1,600 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
已完成
入组人数
1,600

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 17(—)

入选标准

  • All children <18y presenting to the Emergency department or paediatric intensive care unit or other appropriate wards with fever, or a history of fever <72h, or a suspected infection, in whom the attending clinician determines the need for blood sampling. ;Healthy control children: • afebrile control children who are having blood tests for reasons other than for investigation of infectious or inflammatory illness.

排除标准

  • Participation may not lead to an earlier need for blood transfusion.

研究者

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