Skip to content

Intubation and Extubation Over 48 Hours Mechanical Ventilation

Observational Study of Intubation and Extubation Over 48 Hours Mechanical Ventilation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01123681
Acronym
INDEX48
Enrollment
200
Registered
2010-05-14
Start date
2010-05-31
Completion date
Unknown
Last updated
2010-11-16

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

Conditions

Critical Illness, Pneumonia, Ventilator-Associated

Keywords

Respiration, Artificial, Pneumonia, Ventilator-Associated, Critical Illness

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.

Interventions

DEVICEChoice of endotracheal tube

Types of endotracheal tube, normal cuff without sub-glottic aspiration, normal cuff with sub-glottic aspiration, Special cuff with sub-glottic aspiration

Sponsors

Okayama Research Investigator Organizing Network
Lead SponsorNETWORK

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 20 years old * Mechanically ventilated over 48 hours in the ICU

Exclusion criteria

* Mask ventilation * Tracheostomy

Design outcomes

Primary

MeasureTime frameDescription
Occurrence and timing of ventilator associated pneumoniaone monthFrom tracheal intubation to ICU duscharge

Secondary

MeasureTime frameDescription
Ventilator-free daysone monthDuring ICU stay
Duration of ICU stay and hospital staythree monthsFrom tracheal intubation to ICU or hospital discharge
ICU and hospital mortalitythree monthsFrom tracheal intubation to hospital discharge

Countries

Japan

Outcome results

None listed

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