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临床试验/NCT00148642
NCT00148642已完成3 期

Multi-center Clinical Trial of the Bard Silver-coated Endotracheal Tube to Reduce Ventilator Associated Pneumonia (VAP)

C. R. Bard10 个研究点 分布在 1 个国家目标入组 2,003 人开始时间: 2002年11月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
2,003
试验地点
10
主要终点
The incidence of microbiologically-confirmed VAP (mVAP), as determined by quantitative culture of bronchoalveolar lavage fluid, in subjects intubated for >=24 hours.

研究概览

简要总结

The purpose of this study is to determine if the use of a silver-coated endotracheal tube (ETT) can reduce the incidence and/or delay the time of onset of VAP when compared to a non silver-coated ETT in patients who have been mechanically ventilated for >= 24 hours.

详细描述

Nosocomial pneumonia is the leading cause of death from hospital-acquired infections.Ventilator associated pneumonia (VAP) develops in a significant percentage of patients who have been ventilated for at least 48 hours, and is associated with high morbidity, mortality,and financial costs. Silver is a well-characterized antimicrobial agent, and is the active agent in multiple medical products used to reduce or control infection. Bard has developed a proprietary antimicrobial ETT, manufactured with a hydrophilic coating containing a fine dispersion of silver salts.

This study compare the incidence and time to onset of VAP in patients intubated for >=24 hours with a proprietary silver-coated ETT versus those intubated for >= 24 hours with a standard non-coated ETT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Participant, 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

  • age > 18 years
  • expected to be intubated for at least 24 hours
  • able to sign Informed Consent

排除标准

  • symptoms of bronchiectasis
  • severe hemoptysis
  • history of cystic fibrosis
  • intubated > 12 hours within previous 30 days
  • pregnancy
  • participating in a competing trial

结局指标

主要结局

The incidence of microbiologically-confirmed VAP (mVAP), as determined by quantitative culture of bronchoalveolar lavage fluid, in subjects intubated for >=24 hours.

时间窗: 30 days

次要结局

  • time to onset of mVAP in subjects intubated for >=24 hours(30 days)
  • duration of intubation(unlimited)
  • mortality(unlimited)
  • antibiotic usage(unlimited)
  • length of stay(unlimited)
  • incidence of clinical VAP in subjects intubed for >=24 hours(30 days)

研究者

发起方
C. R. Bard
申办方类型
Industry

研究点 (10)

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