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临床试验/NL-OMON35587
NL-OMON35587已完成2 期

Pain treatment of newborns: paracetamol rectal versus intraveneous administration, an open randomised clinical trial. - Pain treatment of newborns:paracetamol rectal versus iv administration

Vrije Universiteit Medisch Centrum0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
24

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

  • 1. gestational age > 26 weeks
  • 2. weight at birth for gestational age < p97
  • 3. necessity for pain treatment (Comfortneoscore >/<= 14)
  • A minimum of 48 hours persistent pain treatment is required

排除标准

  • 1. no necessity for pain treatment
  • 2. macrosomia (weight at birth > p 97)
  • 3. (severe) congenital abnormalities
  • 4. less than 48 hours pain treatment is required
  • 5. neonates are sedated or paralysed (Comfortneoscore impossible)
  • 6. severe asphyxia (Apgar score < 4 after 5 minutes)
  • 7. hepatic- and renal failure (at first blood screening)
  • 8. rectal blood loss
  • 9. necrotizing enterocolitis (active fase)
  • 10. severe thrombocytopenia (< 50 x 10 9/l)

研究者

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