Weaning From Nasal High Flow Therapy
NCT05210881 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 62
Last updated 2022-01-27
Summary
Nasal high flow is widely used in critically ill patients admitted to the intensive care unit (ICU) for acute hypoxemic respiratory failure. It has been shown to improve patient comfort, increase oxygenation and reduce need for intubation in some patients. The Respiratory Oxygenation (ROX) index has been established as a simple tool to help clinicians identify those patients who will succeed and those who will fail under nasal high flow and therefore predict the need for intubation. However, when nasal high flow therapy is successful, little is known as to how and when weaning of this device should be performed and what are the predictors of a safe withdrawal of the device. The objectives of this retrospective exploratory study are to identify a cut-off value of the ROX index predictive of success of the withdrawal trial, to describe a one-year use of the withdrawal trial; to describe the ROX value closest to weaning from nasal high flow, and to identify factors associated with success or failure of the withdrawal trial from nasal high flow therapy in patients receiving nasal high flow therapy.
Conditions
- Respiratory Distress Syndrome, Adult
- Acute Hypoxemic Respiratory Failure
- Acute Respiratory Distress Syndrome
- Weaning Failure
Sponsors & Collaborators
-
Hôpital Louis Mourier
lead OTHER
Principal Investigators
-
Jean-Damien Ricard, MD, PhD · Assistance Publique - Hôpitaux de Paris
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-01-01
- Primary Completion
- 2019-12-31
- Completion
- 2021-08-31
Countries
- France
Study Locations
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