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临床试验/NL-OMON53465
NL-OMON53465招募中4 期

The effect of antenatal acetaminophen administration on breathing effort of premature infants at birth: a pilot study - AIR study

eids Universitair Medisch Centrum0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中
入组人数
40

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
0 至 0(—)

入选标准

  • - Pregnant women expected to deliver between 24+0-29+6 weeks* gestation and
  • admitted to the Leiden University Medical Centre (LUMC).
  • - Informed consent from caregiver(s)

排除标准

  • - Fetuses with congenital anomalies affecting the heart, lungs, kidneys or
  • - Pregnant women in whom the use of paracetamol is contraindicated for any
  • reason, consisting of: severe renal impairment, severe hepatic impairment,
  • severe active liver disease (including HELLP-syndrome), a known alcohol
  • addiction and a known hypersensitivity to acetaminophen or to any of the
  • excipients in the intravenous formulation.
  • - Pregnant women that use one of the following medication: probenecid,
  • salicylamide, rifampicin, isoniazid, barbiturates, tricyclic antidepressants,
  • anti-epileptic medication, zidovudine, oral coagulants, metoclopramide,
  • domperidone, colestyramine and imatinib.
  • - Acetaminophen administration required for standard care within 4 hours prior
  • - Decision to give palliative care to the neonate.

研究者

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