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Effects of Tracheal Intubation on Ventilation With a Laryngeal Mask During Percutaneous Dilatation Tracheostomy

Effects of Short- and of Long-term Tracheal Intubation on Ventilation With a Laryngeal Mask During Percutaneous Dilatation Tracheostomy.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00771784
Enrollment
60
Registered
2008-10-13
Start date
2008-07-31
Completion date
2010-07-31
Last updated
2012-08-22

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

Conditions

Neurological Diseases, Heart or Respiratory Failure,, Sepsis, Trauma.

Keywords

Endotracheal intubation, tracheostomy, laryngeal mask

Brief summary

The length of tracheal intubation may affect the subsequent ventilation with a laryngeal mask during percutaneous tracheostomy.

Detailed description

Percutaneous tracheostomy is routinely performed while patients are being ventilated with a laryngeal mask. The efficacy of ventilation during tracheostomy may be affected by length of previous endotracheal intubation. This is an observational and monocentric study aimed to evaluate the impact of length of endotracheal intubation on efficacy of lung ventilation with a laryngeal mask. Two groups of patients who have to undergo elective percutaneous tracheostomy after either a short or long endotracheal intubation will be enrolled. Data on the correlational effects of the endotracheal tube on the integrity of laryngeal structures and on ventilation will be collected. Statistical analyses will use standard tests to compare the two groups of patients.

Interventions

None listed

Sponsors

University of Padova
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* age 18-80 years * mechanical ventilation * need of percutaneous tracheostomy

Exclusion criteria

* previous pathologies of upper airways or of oesophagus * risk of bleeding * need of FiO2 \>70% and/or of PEEP \>10 cm H2O * difficult insertion of laryngeal mask * impossibility of endoscopic visualization of the laryngeal structures

Design outcomes

Primary

MeasureTime frame
Ventilatory parameters during percutaneous tracheostomyThirty minutes.

Secondary

MeasureTime frame
Scoring of laryngeal lesions, blood gas exchange, morbidity, mortality.Thirty minutes.

Countries

Italy

Outcome results

None listed

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