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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2007 by University Hospital, Alexandroupolis.
Recruitment status was:  Recruiting
Information provided by:
University Hospital, Alexandroupolis Identifier:
First received: March 21, 2007
Last updated: NA
Last verified: March 2007
History: No changes posted
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 Intervention Phase
Aspiration of Subglottic Secretions
Device: Hi-Lo Evac Endotracheal Tube
Phase 4

Study Type: Observational
Study Design: Allocation: Random Sample
Primary Purpose: Screening
Time Perspective: Cross-Sectional
Time Perspective: Prospective
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

Further study details as provided by University Hospital, Alexandroupolis:

Estimated Enrollment: 60
Study Start Date: January 2007
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.

Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
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
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Please refer to this study by its identifier: NCT00450476

Contact: Christos K Dragoumanis, MD, PhD 00302551075085

University General Hospital of Alexandroupolis Recruiting
Alexandroupolis, Evros, Greece, 68100
Principal Investigator: Christos K Dragoumanis, MD, PhD         
Sub-Investigator: Vassilios Papaiannou, MD, PhD         
Sub-Investigator: Dimitrios Konstantonis, MD, PhD         
Sponsors and Collaborators
University Hospital, Alexandroupolis
Principal Investigator: Christos K Dragoumanis, MD, PhD Intensive Care Unit, University Hospital of Alexandroupolis
  More Information Identifier: NCT00450476     History of Changes
Other Study ID Numbers: 30/3/25-01-2007
Study First Received: March 21, 2007
Last Updated: March 21, 2007

Keywords provided by University Hospital, Alexandroupolis:
ventilator associated pneumonia
endotracheal intubation
mechanical ventilation processed this record on April 28, 2017