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临床试验/NL-OMON49787
NL-OMON49787已完成不适用

Procalcitonin as parameter for neonatal infection - Pro-EOS study

Spaarne Gasthuis0 个研究点目标入组 180 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
180

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 11(—)

入选标准

  • Amenorrhea of >= 32 weeks, age <7 days old
  • - Neonates that had one or more prenatal risk factors for neonatal infection
  • according to table 2b in the NVK early-onset neonatal infection protocol, OR
  • neonates that are admitted with a suspected infection <7 days postpartum.

排除标准

  • (Suspected) chromosomal abnormalities or severe congenital anomalies.
  • Neonates born in an other hospital/neonates who have been admitted to another
  • hospital in the past.

研究者

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Procalcitonin as parameter for neonatal infectio | 临床试验