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Weaning Protocol for High-flow Nasal Oxygen Therapy in Intensive Care

Abroad (travel likely)Recruiting

Conditions

Acute Hypoxemic Respiratory Failure · High-flow Nasal Oxygen Therapy

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • Intensive care, University Hospital, Blois, Blois, France

    Contact: Study coordinator (Julien GROUILLE, MD)
    Contact: Principal Investigator (Julien GROUILLE)

  • Intensive care unit, University Hospital, Bourg-en-Bresse, Bourg-en-Bresse, France

    Contact: Study coordinator (Salman Mohammad)
    Contact: Principal Investigator (Salman MOHAMMAD)

  • Intensive care, University Hospital, Bourges, Bourges, France

    Contact: Study coordinator (Anna BOURREAU, MD)
    Contact: Principal Investigator (Anna BOURREAU)

  • Intensive care unit, University Hospital, Caen, Caen, France

    Contact: Study coordinator (Pierrick BAUDUIN) · bauduin-p@chu-caen.fr · 0662885851
    Contact: Principal Investigator (Pierrick BAUDUIN)

  • Intensive care, University Hospital, Chartres, Chartres, France

    Contact: Study coordinator (Juliette AUDIBERT, MD)
    Contact: Principal Investigator (Juliette AUDIBERT)

  • Intensive care, University Hospital, Cholet, Cholet, France

    Contact: Study coordinator (Fabien JAROUSSEAU, MD)
    Contact: Principal Investigator (Fabien JAROUSSEAU)

  • Intensive care, University Hospital, Dax, Dax, France

    Contact: Study coordinator (Adrien AUVET, MD)
    Contact: Principal Investigator (Adrien AUVET)

  • Intensive care, University Hospital, Le Mans,, Le Mans, France

    Contact: Study coordinator (Mickael LANDAIS, MD)
    Contact: Principal Investigator (Mickael LANDAIS)

  • Intensive care, University Hospital, Orléans, Orléans, France

    Contact: Study coordinator (Mai-Anh NAY, MD)
    Contact: Principal Investigator (Mai-Anh NAY)

  • Intensive care, University Hospital, Tours, Tours, France

    Contact: Study coordinator (Sophie JACQUIER, MD)
    Contact: Principal Investigator (Sophie JACQUIER)

  • Intensive care unit, University Hospital, Vannes, Vannes, France

    Contact: Study coordinator (Agathe DELBOVE, MD)
    Contact: Principal Investigator (Agathe DELBOVE)
Study leads

  • Mai-Anh NAY, MD

    Principal Investigator

    CHRU Orléans

View source on ClinicalTrials.gov(opens in a new tab)