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

U

University Hospital, Alexandroupolis

Status

Unknown

Conditions

Aspiration of Subglottic Secretions

Treatments

Device: Hi-Lo Evac Endotracheal Tube

Study type

Observational

Funder types

Other

Identifiers

NCT00450476
30/3/25-01-2007

Details and patient eligibility

About

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.

Full 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.

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

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

Trial contacts and locations

1

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Central trial contact

Christos K Dragoumanis, MD, PhD

Data sourced from clinicaltrials.gov

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