Breathing tube biofilm study aims to unlock pneumonia prevention
NCT ID NCT04926493
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study looked at the buildup of germs (biofilm) on breathing tubes in 61 ICU patients who were on ventilators for more than 2 days. The goal was to better understand how this biofilm might be linked to ventilator-associated pneumonia. Researchers analyzed the structure and germs in the biofilm to find clues for future prevention.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could point toward better ways to prevent ventilator-associated pneumonia in ICU patients.
- What could go wrong
- This is an observational study, not a treatment trial. It aims to gather knowledge, not test a therapy, so direct patient benefits are not guaranteed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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61 people
The number who actually took part.
- Started
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May 2021
- Finished
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Jul 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patient \> 18 years of age with mechanical ventilation for \>2 calendar days
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patient \> 18 years of age with mechanical ventilation for \>2 calendar days Exclusion Criteria: * inability to collect or dispatch the endotracheal tube for proper characterization within 24 hours post-extubation
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU Dijon Bourgogne
Dijon, 21000, France
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Other studies related to the condition(s) this trial covers.
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