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临床试验/NCT03449056
NCT03449056Unknown3 期

High-flow Nasal Cannula Nebulization of Beta 2 Adrenergic Agonist During Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Poitiers University Hospital1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2019年1月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
25
试验地点
1
主要终点
compare lung functions

研究概览

简要总结

High-flow nasal cannula is an oxygenation technique increasingly used for patients admitted for acute respiratory failure. Literature essentially concerns "de novo" acute hypoxemic failure and the interest of high-flow during take care of chronic obstructive pulmonary disease patients is few studied. Physiological studies reported potential benefits of high-flow nasal cannula oxygenation in chronic obstructive pulmonary disease patients including dead space clearance and decrease of respiratory, which lead to decrease work of breathing. As inhaled bronchodilators are part of treatment of chronic obstructive pulmonary disease exacerbation, nebulization could be also provided through high-flow nasal cannula oxygen therapy. The aim of our study is to determine whether a beta-2 agonist nebulization administered through High-flow nasal cannula is efficient to improve spirometry of patients for admitted hronic obstructive pulmonary disease exacerbation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Arterial pH over 7.25,
  • Respiratory rate under 35 breaths/mn
  • Glasgow Coma Scale equal to 15,
  • indication of beta-2 agonist nebulization less than 8 per day (time between two nebulization more than 3 hours),
  • NIV sessions spaced more than 6 hours.

排除标准

  • Urgent endotracheal intubation;
  • Contraindication to beta 2 adrenergic agonist;
  • Another organ failure (hemodynamic and neurological instability);
  • Cardioselective beta-blocker during treatment of copd exacerbation;

研究组 & 干预措施

TREATMENT

Experimental

salbutamol nebulization

干预措施: salbutamol (Drug)

结局指标

主要结局

compare lung functions

时间窗: baseline-1h30

Evolution of Forced Expiratory Volume 1s

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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