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Clinical Trials/NCT00450476
NCT00450476
Unknown
Not Applicable

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

University Hospital, Alexandroupolis1 site in 1 country60 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aspiration of Subglottic Secretions
Sponsor
University Hospital, Alexandroupolis
Enrollment
60
Locations
1
Last Updated
19 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
TBD
Last Updated
19 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Alexandroupolis

Eligibility Criteria

Inclusion Criteria

  • Critically ill patients with orotracheal intubation and anticipated duration of intubation more than 48 hours

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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