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

Sponsor
University Hospital, Alexandroupolis (Other)
Overall Status
Unknown status
CT.gov ID
NCT00450476
Collaborator
(none)
60
1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Hi-Lo Evac Endotracheal Tube

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.

Study Design

Study Type:
Observational
Time Perspective:
Other
Official Title:
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
Study Start Date :
Jan 1, 2007

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Critically ill patients with orotracheal intubation and anticipated duration of intubation more than 48 hours

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University General Hospital of Alexandroupolis Alexandroupolis Evros Greece 68100

    Sponsors and Collaborators

    • University Hospital, Alexandroupolis

    Investigators

    • Principal Investigator: Christos K Dragoumanis, MD, PhD, Intensive Care Unit, University Hospital of Alexandroupolis

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00450476
    Other Study ID Numbers:
    • 30/3/25-01-2007
    First Posted:
    Mar 22, 2007
    Last Update Posted:
    Mar 22, 2007
    Last Verified:
    Mar 1, 2007

    Study Results

    No Results Posted as of Mar 22, 2007