Silver-Coated Endotracheal Tube to Reduce Ventilator Associated Pneumonia (VAP)



Status:Completed
Conditions:Pneumonia, Pneumonia, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:November 2002
End Date:March 2006

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

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.

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.

Inclusion Criteria:

- age > 18 years

- expected to be intubated for at least 24 hours

- able to sign Informed Consent

Exclusion Criteria:

- symptoms of bronchiectasis

- severe hemoptysis

- history of cystic fibrosis

- intubated > 12 hours within previous 30 days

- pregnancy

- participating in a competing trial
We found this trial at
5
sites
Oak Park, Illinois 60302
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Oak Park, IL
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Rochester, Minnesota 55905
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Rochester, MN
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San Antonio, TX
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San Diego, California 92093
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San Diego, CA
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St. Louis, Missouri 63141
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St. Louis, MO
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