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临床试验/NCT01281748
NCT01281748终止4 期

Evaluation Of The Efficacy Of Corticosteroids In Patients With An Acute Exacerbation Of Chronic Obstructive Pulmonary Disease Receiving Ventilator Support

Hospital Universitario Getafe1 个研究点 分布在 1 个国家目标入组 83 人开始时间: 2005年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
发起方
入组人数
83
试验地点
1
主要终点
Duration of mechanical ventilation

研究概览

简要总结

Clinical practice guidelines for the management of chronic obstructive pulmonary disease (COPD) recommend treatment with systemic corticosteroids during acute exacerbations. The results of a Cochrane systematic review show that treatment with systemic corticosteroids improves lung function over the first 72 hours of an exacerbation of COPD but the effect on other outcomes, particularly length of hospital stay, is unclear, so further research should be directed at determining the risk-benefit ratio, particularly those at high risk of developing adverse drug reactions. In critically ill patients, corticosteroid treatment is a risk factor of infections, hyperglucemia and critical-illness neuromuscular abnormalities, and these conditions are associated with an increased morbidity and mortality. The effect of treatment with systemic corticosteroids in COPD patients with acute exacerbation requiring mechanical ventilation has not been evaluated investigated so it is unknown if the corticosteroids could reduce the duration of mechanical ventilation and the length of intensive care unit (ICU) stay or if, on the contrary, the development of adverse events could lead to a longer time on mechanical ventilation and ICU stay.

PRIMARY OBJECTIVES: To evaluate the effect of corticosteroids on the duration of mechanical ventilation, the length of ICU stay, the need for tracheal intubation in patients treated with non-invasive mechanical ventilation. To evaluate the frequency of adverse events: secondary infections, pneumonia, arterial hypertension, hyperglucemia, gastrointestinal bleeding, and critical-illness neuromuscular abnormalities. DESING: Multicenter, prospective, randomized, double blind, placebo-controlled clinical trial.The treatment group will receive intravenous methylprednisolone for 10 days and the control group will receive isotonic saline solution.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Adult patients (age > 18 years) admitted to participating ICUs with:
  • Primary diagnosis of COPD exacerbation defined as the presence of two or more of the following clinical features: worsening dyspnea, increase in sputum purulence, increase in sputum volume
  • respiratory failure [pH < 7,35 with a PaCO2 > 45 mm Hg and respiratory rate more than 23 breaths per minute] requiring mechanical ventilation, invasive or non-invasive mechanical ventilation.

排除标准

  • Primary diagnosis of asthma exacerbation.
  • History of asthma or atopy.
  • Use of systemic corticosteroids within the preceding month.
  • Use of systemic corticosteroids for the treatment of COPD exacerbation at the time of ICU admission for more than 24 hours.
  • Clinical or radiological evidence of pneumonia.
  • Uncontrolled left-ventricular failure (patients with evidence of severe heart failure requiring inotropes or vasoactive drugs).
  • Uncontrolled hypertension arterial (systolic pressure > 180 mm Hg or diastolic pressure > 90 mm Hg despite antihypertensive therapy).
  • Uncontrolled diabetes mellitus.
  • Presence of a neuromuscular disease.
  • History of allergy and or adverse reaction to corticosteroids.

研究组 & 干预措施

methylprednisolone

Experimental

干预措施: intravenous methylprednisolone (Drug)

normal saline solution

Placebo Comparator

干预措施: intravenous normal saline solution (Other)

结局指标

主要结局

Duration of mechanical ventilation

时间窗: Participants are followed until ICU discharge

Time elapsed between tracheal intubation and extubation (in the group of patients treated with invasive mechanical ventilation),or time elapsed between initiation of non-invasive mechanical ventilation and withdrawal of non-invasive mechanical ventilation (in the group of patients successfully treated with non-invasive mechanical ventilation, or time elapsed between initiation of non-invasive ventilation and extubation (in the case of those patients who failed non-invasiev ventilation and required tracheal intubation).

Need for intubation in patients treated with non-invasive mechanical ventilation

时间窗: Participants are followed until ICU discharge

Number of patients intubated in the following 48 hours after the initiation of non-invasive mechanical ventilation

Length of ICU stay

时间窗: Participants are followed until ICU discharge

Time elapsed between ICU admission and ICU discharge (dead or alive)

次要结局

  • ICU mortality(Participants are followed until ICU discharge)
  • Length of hospital stay(Participants are followed until hospital discharge)

研究者

发起方
Hospital Universitario Getafe
申办方类型
Other

研究点 (1)

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