跳至主要内容
临床试验/NCT02112305
NCT02112305Unknown不适用

Comparison Efficacy of Nebulized Magnesium Sulphate to Intravenous Magnesium Sulphate in Children With Severe Acute Asthma

Queen Sirikit National Institute of Child Health1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
40
试验地点
1
主要终点
Asthma severity score

研究概览

简要总结

The purpose of this study is to determine whether nebulized magnesium sulphate is effective in the treatment of acute severe asthma when comparison with intravenous magnesium sulphate

详细描述

Intervention: At randomization eligible patients were allocated to receive 2.5ml of isotonic magnesium sulphate (150 mg,245 mmol/L) on three occasional at 20 minutes interval or standard treatment 50 mg/kg intravenous magnesium sulphate. The asthma severity score was record at 0,20,40,60,120,180,240 minutes post randomization. Adverse event were assessed at each assessment point. Patients were followed up until discharge from hospital to collect secondary outcome data.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children age 2-15 years presenting with severe asthma or persistent wheeze without responding to conventional therapy

排除标准

  • chronic lung disease
  • history of adverse reaction form magnesium sulphate
  • life threatening condition

研究组 & 干预措施

isotonic magnesium sulphate

Experimental

2.5 ml of isotonic magnesium sulphate (150 mg, 245 mmol/L) on three occasional at 20 minutes interval

干预措施: isotonic magnesium sulphate (Drug)

50% magnesium sulphate

Active Comparator

magnesium sulphate 50mg/kg/dose intravenous drip in 20 minutes for one dose

干预措施: 50% magnesium sulphate (Drug)

结局指标

主要结局

Asthma severity score

时间窗: 60 minute

次要结局

  • Length of stay in the hospital(within 2 weeks)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Tassalapa Daengsuwan

medical doctor

Queen Sirikit National Institute of Child Health

研究点 (1)

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