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临床试验/CTRI/2017/11/010663
CTRI/2017/11/010663已完成未知

To determine the effect of intravenous in-line filters on morbidity and mortality in neonates.

none0 个研究点目标入组 328 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
328

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • all newborn babies (30 - 36 wk of gestation ) , mother without any antenatal risk factor for sepsis,admitted at llrm within 1 -6 hours of life

排除标准

  • Babies with any of the following will be excluded:
  • 1).Babies born with any major congenital anomalies.
  • 2).Very preterm babies or extremely low birth weight babies
  • ( < 30 weeks and birth weight <1.2kg)
  • 3). Babies with Severe perinatal asphyxia
  • 4).Babies with severe sepsis at the time of admission.
  • 5).Babies delivered by mothers with antenatal risk factors for sepsis.
  • 6).Extra mural babies (after 6 hours of life &previous hospitalization)

研究者

发起方
none

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