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临床试验/NCT02200185
NCT02200185已完成不适用

Efficacy and Safety of Nebulized Morphine Given at Two Different Doses Compared to Intravenous Morphine in Post-traumatic Acute Pain: a Randomized Controlled Double Blind Study

University of Monastir1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2012年4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
状态
已完成
入组人数
300
试验地点
1
主要终点
Pain resolution

研究概览

简要总结

The investigators test a different technique using morphine to improve pain relief in patient visiting the emergency department with acute trauma pain, for this we are comparing three different methods of morphine administration:

  • intravenous titrated morphine
  • low dose nebulized morphine and
  • high dose nebulized morphine

详细描述

Trauma patients are frequent in emergency department settings, and often require urgent care.

taking care of this patients consists on taking care of their pain and then the specific treatment of their traumatic lesions.

actually, the most used medicine and most efficient one in treating pain is morphine, it's mechanism of action is by acting on receptors located on neuronal cell membranes and inhibit neurotransmitter release.

The most applied administration root of morphine is by intravenous (IV) titration or IV continuous perfusion, but until now, there is no clear recommendation concerning the superiority of this root over other administration techniques such as nebulization.

In this study we aimed to investigate the efficiency, the feasibility and the tolerance of three morphine administration roots in patients with acute traumatic pain and to clarify the most adequate one to apply in emergency department settings.

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
Double (Participant, Care Provider)

入排标准

年龄范围
8 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • patients older than 8 years and less than 50 years
  • patients who consult emergency department for sever pain after an immediately trauma

排除标准

  • Glasgow coma scale <14
  • inability to cooperate
  • hypotension with systolic blood pressure< 90mmhg
  • bradypnea<12cpm
  • SAO2<90%
  • polytrauma
  • nasal trauma
  • nasal obstruction
  • allergy to opioids

研究组 & 干预措施

IV titrated morphine

Placebo Comparator

patient will receive 2 mg morphine each 5 min, associated to continuous nebulisation of saline serum (placebo).

Morphine administration is stopped when VAS becomes under 50% and treatment failure is defined as VAS > 50%, 30 minutes after the beginning of the protocol.

干预措施: IV titrated morphine (Drug)

Low dose nebulised morphine

Experimental

patient will receive 10 mg of morphine prepared with 4 ml saline serum (SS) and nebulised with 6 l/min flow during 10 minutes.

Nebulisation will be repeated 3 times, in addition, patients receive 2 ml IV SS every 5 minutes as placebo

干预措施: Low dose nebulised morphine (Drug)

High dose nebulised morphine

Experimental

patient will receive 20 mg of morphine prepared with 3 ml saline serum (SS) and nebulised with 6 l/min flow during 10 minutes.

Nebulisation will be repeated 3 times, in addition, patients receive 2 ml IV SS every 5 minutes as placebo.

干预措施: High dose nebulised morphine (Drug)

结局指标

主要结局

Pain resolution

时间窗: 30 minutes

primary end point defined by the decrease in intensity pain objectified by a decline in visual analogy pain scale greater than or equal to 50% of its initial value

次要结局

  • side effects(30 minutes)

研究者

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

Nouira

Professor

University of Monastir

研究点 (1)

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