Status:

COMPLETED

Prediction of PaO2 Values Using the PRoPERLy II Database

Lead Sponsor:

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Conditions:

Invasive Ventilation

Eligibility:

All Genders

16-99 years

Brief Summary

Four prospective observational studies of ventilation in critically ill patients were harmonized and pooled.

Detailed Description

The individual data from four observational studies ('Epidemiology of Respiratory Insufficiency in Critical Care study' \[ERICC\], the 'Large Observational Study to Understand the Global Impact of Sev...

Eligibility Criteria

Inclusion

  • ERICC included patients aged 18 years or older that received ventilatory support for at least 24 hours during the first 48 hours of ICU admission at the participating ICUs. ERICC excluded patients with a tracheostomy, patients admitted for routine uncomplicated postoperative care, readmissions and patients with a terminal condition. ERICC enrolled patients during 2-months period.
  • LUNG SAFE included patients aged 16 years or older that received invasive or noninvasive ventilation. LUNG SAFE excluded patients without informed consent. LUNG SAFE enrolled patients during a 4-week period in the winter months.
  • PRoVENT included patients aged 18 years or older that received invasive ventilation. PRoVENT excluded patients in whom ventilation was started before the study recruitment week, patients receiving only noninvasive ventilation, and patients that were transferred to the ICU from another hospital under ventilation. PRoVENT enrolled patients during 4-week period.
  • PRoVENT-iMiC included patients aged 18 years or older that started with invasive ventilation. They excluded patients that received only noninvasive ventilation, patients whose invasive ventilation started before the inclusion phase of the study, and patients transferred from another hospital while under ventilation. PRoVENT-iMiC enrolled patients during 4-week period.

Exclusion

    Key Trial Info

    Start Date :

    January 1 2024

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    July 26 2024

    Estimated Enrollment :

    8000 Patients enrolled

    Trial Details

    Trial ID

    NCT06589427

    Start Date

    January 1 2024

    End Date

    July 26 2024

    Last Update

    September 19 2024

    Active Locations (1)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (1 locations)

    1

    Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    Amsterdam, Netherlands