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Intubation and Extubation Over 48 Hours Mechanical Ventilation

Conditions
Pneumonia, Ventilator-Associated
Critical Illness
Interventions
Device: Choice of endotracheal tube
Registration Number
NCT01123681
Lead Sponsor
Okayama Research Investigator Organizing Network
Brief Summary

The purpose of this study is to determine how often ventilator associated pneumonia happens in the current intensive care units, and how types of endotracheal tube affect its occurrence.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Age > 20 years old
  • Mechanically ventilated over 48 hours in the ICU
Exclusion Criteria
  • Mask ventilation
  • Tracheostomy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Ventilator associated pneumoniaChoice of endotracheal tube-
No pneumoniaChoice of endotracheal tube-
Primary Outcome Measures
NameTimeMethod
Occurrence and timing of ventilator associated pneumoniaone month

From tracheal intubation to ICU duscharge

Secondary Outcome Measures
NameTimeMethod
Ventilator-free daysone month

During ICU stay

Duration of ICU stay and hospital staythree months

From tracheal intubation to ICU or hospital discharge

ICU and hospital mortalitythree months

From tracheal intubation to hospital discharge

Trial Locations

Locations (6)

Intensive Care Unit, Himeji Red Cross Hospital

🇯🇵

Himeji, Hyogo, Japan

Intensive Crae Unit, Kochi Medical School Hospital

🇯🇵

Kochi, Japan

Intensive Care Unit, Kagawa Rosai Hospital

🇯🇵

Marugame, Japan

Intensive Care Unit, Hiroshima City Hospital

🇯🇵

Hiroshima, Japan

Intensive Care Unit, Tsuyama Chuo Hospital

🇯🇵

Tsuyama, Japan

Intensive Care Unit, Okayama University Hospital

🇯🇵

Okayama, Japan

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