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Evaluation of the efficacy of a newly developed endotrachel tube

Evaluation of the sealing effect of a newly developed endotracheal tube in a small cohort of mechanically ventilated critically ill patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29558
Enrollment
10
Registered
2014-04-07
Start date
2014-09-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

endotracheal tube, tracheal sealing, double cuff, ventilator-associated pneumonia, prevention

Interventions

Patients are intubated lege arte by an experienced intensivist/anesthesiologist. Appropriate sedoanalgesia (midazolam, propofol and remifentanil) and muscle paralysis (atracurium), if required, is adm

Sponsors

University Hospital Brussels
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: mechanically ventilated patients > 18 years, electively intubated with the novel ETT

Exclusion criteria

Exclusion criteria: - patients ventilated for < 24h - refusing informed consent

Design outcomes

Primary

MeasureTime frame
If on any occasion a blue spot is observed on the trachel mucosa caudal to the tube’s tip, leakage will be confirmed and the experiment ended.

Secondary

MeasureTime frame
Throughout the experiment, following items are carefully and continuously evaluated: tube localization in the trachea (standard chest X-ray, fibroscopy), interaction with ventilation and humidification (monitoring of in- and expiratory tidal volume and airway pressures), effect of common manipulations (tracheal aspiration, transport, airway care, disconnection of ventilator, eventual weaning,…)

Contacts

Public ContactH. Spapen

Intensive Care Unit, University Hospital Brussels Laarbeeklaan 101

herbert.spapen@uzbrussel.be+32-2-4775178

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)