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
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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