跳至主要内容
临床试验/NCT00243828
NCT00243828终止4 期

Assessment of the Effectivity of Total-face Mask for Noninvasive Ventilation During Acute Respiratory Failure: a Randomized Controlled Trial.

Corporacion Parc Tauli1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2005年11月1日最近更新:
适应症

试验速览

阶段
4 期
状态
终止
发起方
入组人数
300
试验地点
1
主要终点
Intubation rate

研究概览

简要总结

Total-face mask may improve the efficacy of NIV compared to conventional face mask in patients with acute respiratory failure due to enhanced tolerance and the allowance of higher airway pressure without massive leaks.MAIN OBJECTIVE: To assess, in acute respiratory failure patients, whether the total-face mask reduce the intubation rate. METHODS: 300 patients admitted in the ICU for acute respiratory failure needing continuous noninvasive mechanical ventilation. The type of mask (total-face vs. conventional face mask) will be randomized. Defined failure criteria and weaning technique will be used.

详细描述

HYPOTESIS: Total-face mask may improve the efficacy of NIV compared to conventional face mask in patients with acute respiratory failure due to enhanced tolerance and the allowance of higher airway pressure without massive leaks.OBJECTIVES: To assess, in acute respiratory failure patients, whether the total-face mask reduce the intubation rate. Additionally, whether it may improve mask tolerance, skin pressure damage, number of patients receiving higher pressures, or even a reduction in mortality. METHODS: 300 patients admitted in the ICU for acute respiratory failure needing continuous noninvasive mechanical ventilation. The type of mask (total-face vs. conventional face mask) will be randomized. PEEp will be titrated to the best oxygenation and IPAP up to reduce dyspnea and respiratory frequency, with the limits at clinical tolerance and massive leaks. Defined failure criteria and weaning technique will be used. Data to record include clinical parameters and mortality risk score (SAPS II), and physiologic response to NIV (either subjective and objective), technique failures and outcome. EXPECTED RESULTS: The study has been powered to detect a 30% relative improvement in intubation rate from a 35% baseline incidence of intubation in the conventional group.

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

入选标准

  • •Acute Hypoxemia:PaO2/FiO2 lower than 200 mmHg
  • •Respiratory rate greater than 30 breaths/min

排除标准

  • •cardiogenic lung edema
  • •COPD exacerbation
  • •Low level of consciousness (GCS < 13)
  • •Hemodynamic instability
  • •Facial damage
  • •Do-not-intubate orders
  • •Lack of informed consent

结局指标

主要结局

Intubation rate

次要结局

  • Hospital survival

研究者

发起方
Corporacion Parc Tauli
申办方类型
Other

研究点 (1)

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