Trials / Unknown
UnknownNCT00450476
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
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (planned)
- Sponsor
- University Hospital, Alexandroupolis · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Hi-Lo Evac Endotracheal Tube |
Timeline
- Start date
- 2007-01-01
- First posted
- 2007-03-22
- Last updated
- 2007-03-22
Locations
1 site across 1 country: Greece
Source: ClinicalTrials.gov record NCT00450476. Inclusion in this directory is not an endorsement.