跳至主要内容
临床试验/NL-OMON46725
NL-OMON46725已完成4 期

Pediatric Ards Neuromuscular blockade (PAN) study: Life-threatening acute respiratory failure in children: to breathe or not to breathe spontaneously, that's the question. A multicentre, randomised, double-blind, placebo controlled study. - PAN study

niversitair Medisch Centrum Groningen0 个研究点目标入组 178 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
178

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

  • - Informed consent
  • - Age younger than 5 years
  • - Need for invasive mechanical ventilation with PEEP 5 cmH2O
  • - Early moderate - to - severe paediatric acute respiratory distress syndrome originating from any cause:
  • * Acute onset of disease, and
  • * Oxygenation index > 12, and
  • * One or more (bilateral) infiltrates on chest radiograph, and
  • * No evidence of left ventricular failure or fluid overload, and
  • * Within the first 96 hours of PICU admission
  • - Arterial line or central venous line present

排除标准

  • - No informed consent
  • - Known allergy or intolerance to rocuronium
  • - Continuous administration of neuromuscular blockade prior at the time of meeting the criteria for paediatric acute respiratory distress syndrome
  • - Bolus administration of neuromuscular blockade within 1hr before meeting the criteria for paediatric acute respiratory distress syndrome
  • - Chronic respiratory failure on home ventilation
  • - Intracranial hypertension
  • - Bone marrow transplantation
  • - Pre-existing pulmonary hypertension
  • - Congenital heart disease with left - to - right shunting
  • - Cyanotic congenital heart disease
  • - (Suspected) underlying neuromuscular or metabolic disorder
  • - Expected duration of mechanical ventilation less than 48 hours
  • - Withdrawal of life-sustaining treatment or other treatment limitations

研究者

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