Skip to main content
OpenTrials
Completed

NCT Number: NCT01802827

Ventilator Associated Tracheobronchitis in the First 14 Days in ICU

To investigate the clinical course and risk factors for VAT and the impact of VAT on Intensive Care Unit (ICU) morbidity and mortality.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • > 48 hours mechanical ventilation

Exclusion criteria

  • immunodeficiency
  • pregnancy
  • severe COPD, chronic bronchitis, bronchiectasis
  • recent pneumonia

Treatment and study plan

Primary outcomes

  1. mortality

    Time frame: mortality at 4 weeks

    we assessed mortality from all causes at 4 weeks

Secondary outcomes

  1. ICU length of stay

    Time frame: expected average length of stay 15 days

  2. mortality at 6 months

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of Thessaly

Other

Registry information

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Mar 1, 2013
Registry last updated
Mar 1, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.