Clinical Trials Directory

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UnknownNCT00450476

Aspiration of Subglottic Secretions Using Hi-Lo Evac Endotracheal Tube: Tube Size and Incidence of Suction Lumen Dysfunction

Aspiration of Subglottic Secretions in Intubated Critically Ill Patients Using Hi-Lo Evac Endotracheal Tube: Correlation Between Tube Size and Incidence of Suction Lumen Dysfunction

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (planned)
Sponsor
University Hospital, Alexandroupolis · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To evaluate the correlation between endotracheal tube size and incidence of dysfunction of suction lumen of Hi-Lo Evac endotracheal tube in critically ill patients who required mechanical ventilation for more than 48 hours.

Detailed description

In mechanically ventilated patients, aspiration of subglottic secretions is a widely used intervention for prevention of ventilator-associated pneumonia. Using Hi-Lo® Evac endotracheal tube (Hi-Lo Evac; Mallinckrodt; Athlone, Ireland), dysfunction of suction lumen and subsequent failure to aspirate the subglottic secretions is not uncommon. The objective of this prospective observational study is to determine the causes and the incidence of suction lumen dysfunction of Evac endotracheal tube.

Conditions

Interventions

TypeNameDescription
DEVICEHi-Lo Evac Endotracheal Tube

Timeline

Start date
2007-01-01
First posted
2007-03-22
Last updated
2007-03-22

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT00450476. Inclusion in this directory is not an endorsement.