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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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00450476
Enrollment
60
Registered
2007-03-22
Start date
2007-01-31
Completion date
Unknown
Last updated
2007-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aspiration of Subglottic Secretions

Keywords

ventilator associated pneumonia, prevention, endotracheal intubation, mechanical ventilation

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.

Interventions

DEVICEHi-Lo Evac Endotracheal Tube

Sponsors

University Hospital, Alexandroupolis
Lead SponsorOTHER

Study design

Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

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

Countries

Greece

Contacts

Primary ContactChristos K Dragoumanis, MD, PhD
christosdragoumanis@gmail.com00302551075085

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026