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 |
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.
(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.
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
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