PREdicting Failure of Non-inVasIve Ventilatory Support Using Non-invaSIve mONitoring in Non-intubated Patients With Acute Hypoxemic Respiratory Failure or Post-extubation Failure. The PREVISION Study

ConditionsVentilatory Failure Hypoxemic Respiratory Failure Weaning Failure Respiratory

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age18+

SponsorUnity Health Toronto

About this trial

The goal of this observational study is to assess the potential non-invasive tools (e.g. regional ventilation, respiratory muscle response, lung mechanic's parameters) to identify the risk of failure when using high flow nasal cannula (HFNC) or non-invasive ventilation (NIV).

The main question, it aims to answer is:

Does abnormal regional ventilation could predict HFNC or NIV failure?

Eligibility criteria

Qualifiers

Age of ≥ 18 years

Using NIV or HFNC anywhere in the hospital

Disqualifiers

Chronic CO2 retention

Neuromuscular disorder

Requiring home NIV (CPAP or BIPAP)

Tracheostomy

Trial design

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Sponsors and collaborators

Unity Health Toronto

Lead sponsor

Source ClinicalTrials.gov