A single center, observational, prospective study to improve knowledge about non-invasive ventilation, obtaining data about compliance, efficacy, imaging in patients who already receive non-invasive ventilation as standard of care.
Eligibility
Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria:
* treatment with non-invasive ventilation
* informed consent
Exclusion Criteria:
* refusal of informed consent
Primary outcome measure(s)
Number of patients requiring NIV in a large university hospital. Incidence of NIV failure (including patient compliance) and NIV related complications. Imaging (chest ultrasound) in a subgroup of patients before and after receiving NIV. — Outcome measures will be assessed every day and participants will be followed for the duration of hospital stay, an expected average of 1 weeks.
Trial sites (1)
Facility
City
Region
Status
Ospedale San Raffaele di Milano
Milan
Italy
Recruiting
More Università Vita-Salute San Raffaele trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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