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Clinical Trial Summary

Ventilator-associated pneumonia (VAP) remains the most frequent healthcare-associated infection (HAI) in the intensive care unit (ICU) and one of the most critical risk factors associated with both significant morbidity as well as mortality. Although VAP treatment relies on early and appropriate antimicrobial therapy, several preventive measures have been described in the literature in order to limit its incidence and clinical impact in the ICU. Among these, preventing biofilm formation on the inner surface of the endotracheal tube appears to hold promise. Yet there is a lack of clinical relevant data documenting a causal relation between biofilm formation and VAP. Designed to overcome this critical limitation, the BIOPAVIR study intends to provide a better structural and microbiological characterization of endotracheal tube biofilm in critically ill patients at increased risk for the development of VAP in ICU during COVID-19 pandemic.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04926493
Study type Observational
Source Centre Hospitalier Universitaire Dijon
Contact Jean Pierre QUENOT
Phone 03.80.29.36.85
Email jean-pierre.quenot@chu-dijon.fr
Status Recruiting
Phase
Start date May 1, 2021
Completion date July 2021

See also
  Status Clinical Trial Phase
Terminated NCT01853982 - Study of Intravenous Ceftolozane/Tazobactam Compared to Piperacillin/Tazobactam in Ventilator-Associated Pneumonia Phase 3
Suspended NCT04620941 - Use of Reticulocyte Ratio and Neutrophil / Lymphocyte Ratio in the Diagnosis of Ventilator-associated Pneumonia
Completed NCT01808092 - A Study Comparing Ceftazidime-Avibactam Versus Meropenem in Hospitalized Adults With Nosocomial Pneumonia Phase 3