Improving Non-invasive Ventilation
ConditionAcute Respiratory Failure
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorUniversità Vita-Salute San Raffaele
About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
treatment with non-invasive ventilation
informed consent
Disqualifiers
refusal of informed consent
Trial population
All patients with acute respiratory failure treated with non-invasive ventilation who give informed consent about treatment of their clinical data
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
Non-invasive ventilation
Procedure/SurgeryNon-invasive ventilation
Treatment groups
750 Participants
are divided into 1 treatment groupGroup A: NIV1 intervention
Trial outcomes
Primary outcomes
1
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.
Time frame
Outcome measures will be assessed every day and participants will be followed for the duration of hospital stay, an expected average of 1 weeks.Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov