Optimisation of High Flow Oxygen Therapy Settings During Hypoxaemic Respiratory Distress Based on Non-contact Measurement of Lung Volumes by Depth Camera

Recruiting Phase 3 Interventional Study
Hypoxemic Respiratory Failure
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
406 (estimated)
Sponsor
University Hospital, Brest · Other
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About This Trial
The goal of this clinical trial is to validate the interest of a strategy adjusting the flow rate delivered under high-flow oxygen (HFO) therapy according to the lung volumes measured by a new technique, in intensive care patients with hypoxemic respiratory distress (HRD). The main question it aims to answer is: "The use of a technique of measurement of lung pulmonary with adjustement to the flo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with hypoxemic respiratory distress define by the following 4 criteria: * Respiratory rate ≥ 25 breaths per minutes * A ratio of the partial pressure of arterial oxygen (PaO2) to the FiO2 ≤ 300 mmHg while the patient is breathing oxygen at a flow rate of 10 liters per…
Contacts

Laetitia BODENES, Dr

+33 2 30 33 76 78

laetitia.bodenes@chu-brest.fr

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