Clinical Evaluation of FreeO2 (Version 4) in All Patients Receiving Oxygen (FreeO24G)

Laval University

Status: Completed

Conditions: Asthma; Respiratory Failure; Respiratory Disease; Pneumonia; COPD Exacerbation

Treatments: Device: FreeO2

Study type: Interventional

Funder types: Other

Identifiers

NCT03119727

21342

Details and patient eligibility

About

Evaluation of automatic titration of oxygen with a new version of FreeO2 (V4)

Full description

In the previous studies, the investigators used many times automatic titration of oxygen on spontanous breathing patient (FreeO2 device) with a prototype develop in our lab in collaboration with Laval university. In this study, we want to evaluate the new version of the FreeO2 device (V4)

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age > or = 18 years old
• Patient receiving oxygen between 1 to 6 lpm for medical pathology
• Admitted to a medical service for less than 72 hours (emergency room not included)

Exclusion criteria

• Unreliable SpO2 signal
• Emergency or intensive care hospitalization
• Absence of NIV or intubation criteria at baseline
• Sleep apnea not paired
• Long-term Oxygen Therapy
• Active delirium and cognitive impairment preventing informed consent

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Automated oxygen adjustment

Other group

Description:

All patient in this study have automatic oxygen titration and automatic oxygen weanning

Treatment:

Device: FreeO2