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Aspiration of Subglottic Secretions Using Hi-Lo Evac Endotracheal Tube: Tube Size and Incidence of Suction Lumen Dysfunction
This study is currently recruiting participants.
Verified by University Hospital, Alexandroupolis, March 2007
Sponsored by: University Hospital, Alexandroupolis
Information provided by: University Hospital, Alexandroupolis
ClinicalTrials.gov Identifier: NCT00450476
  Purpose

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 IV

U.S. FDA Resources
Study Type: Observational
Study Design: Screening, Cross-Sectional, Random Sample, Prospective Study
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.

  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Critically ill patients with orotracheal intubation and anticipated duration of intubation more than 48 hours
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00450476

Contacts
Contact: Christos K Dragoumanis, MD, PhD 00302551075085 christosdragoumanis@gmail.com

Locations
Greece, Evros
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
Investigators
Principal Investigator: Christos K Dragoumanis, MD, PhD Intensive Care Unit, University Hospital of Alexandroupolis
  More Information

Study ID Numbers: 30/3/25-01-2007
Study First Received: March 21, 2007
Last Updated: March 21, 2007
ClinicalTrials.gov Identifier: NCT00450476  
Health Authority: Greece: Ethics Committee

Keywords provided by University Hospital, Alexandroupolis:
ventilator associated pneumonia
prevention
endotracheal intubation
mechanical ventilation

Study placed in the following topic categories:
Critical Illness
Pneumonia, Ventilator-Associated
Pneumonia

ClinicalTrials.gov processed this record on January 14, 2009