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临床试验/NL-OMON49542
NL-OMON49542招募中3 期

Pentoxifylline dose optimization in preterm neonatal sepsis - Pentoxifylline in neonatal sepsis

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
30

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

年龄范围
2 至 11(—)

入选标准

  • - Neonates with gestational age <30 weeks
  • - suspected of late onset sepsis with blood drawn for blood culture and
  • inflammatory biomarkers
  • - IL-6 > 500 pg/ml and/or CRP > 50 mg/L

排除标准

  • - PTX therapy cannot be started within 24 hours of start of antibiotic
  • - Patients with known major congenital defects (e.g. congenital heart disease,
  • pulmonary, or gastrointestinal anomalies) will also be excluded.
  • - If subjects have IL-6 values exceeding 25000 pg/mL at time of onset they will
  • also be excluded. High IL-6 values represent severe episodes of sepsis and high
  • IL-6 values are associated with high mortality rates.
  • - Patients who already participated in this trial during an earlier episode of
  • late onset sepsis.
  • - Patients with pH below 7 in two consecutive blood samples, with at least 1
  • hour between the blood samples, at start of sepsis episode.

研究者

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