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临床试验/ACTRN12612000418875
ACTRN12612000418875尚未招募不适用

A multi-centre randomised, placebo controlled trial of nebulised heparin in patients with or at risk of developing Acute Respiratory Distress Syndrome, to determine if nebulised heparin improves long term physical function.

St.Vincents Hospital/Institute0 个研究点目标入组 256 人开始时间: 2012年4月13日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
256

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Receiving ventilation via an endotracheal tube
  • Started ventilation via an endotracheal tube yesterday or today
  • Expected to require invasive ventilation for at least all of today and all of tomorrow
  • PaO2 to FiO2 ratio less than 300
  • Active ventilator circuit humidification

排除标准

  • Allergy to heparin; any history of heparin induced thrombocytopenia
  • Platelet count less than 50 x 109/L; activated partial thromboplastin time (APTT) is prolonged to greater than 80 seconds and this is not due to anticoagulant therapy
  • Uncontrolled bleeding; pulmonary bleeding during this hospital admission; any history of intracranial, spinal or epidural haemorrhage
  • Neurosurgical procedures during this hospital admission or such procedures are planned; an epidural catheter is in place
  • Hepatic encephalopathy or any history of gastrointestinal bleeding due to portal hypertension or biopsy proven cirrhosis with documented portal hypertension
  • Tracheostomy in place; usually receives home oxygen; usually receives any type of assisted ventilation at home e.g. continuous positive airway pressure for obstructive sleep apnoea
  • Cervical spinal cord injury associated with reduced long-term ability to breathe independently; spinal or peripheral nerve disease with a likely prolonged reduction in the ability to breathe independently e.g. Guillain-Barre syndrome, motor neurone disease
  • Receiving high frequency oscillation ventilation or extra corporeal membrane oxygenation
  • Pregnant or might be pregnant
  • Treatment limits restrict the provision of renal replacement therapy, inotropes, vasopressors or prolonged invasive ventilation; usually treated with haemodialysis or peritoneal dialysis for end-stage renal failure; dementia; death is deemed imminent or inevitable or there is underlying disease with a life expectancy of less than 90 days

研究者

发起方
St.Vincents Hospital/Institute

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