Improving Non-invasive Ventilation
Recruiting
- Conditions
- Acute Respiratory Failure
- Interventions
- Procedure: Non-invasive ventilation
- Registration Number
- NCT01571986
- Lead Sponsor
- Università Vita-Salute San Raffaele
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 750
Inclusion Criteria
- treatment with non-invasive ventilation
- informed consent
Exclusion Criteria
- refusal of informed consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description NIV Non-invasive ventilation All patients with acute respiratory failure treated with non-invasive ventilation who give informed consent about treatment of their clinical data
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ospedale San Raffaele di Milano
🇮🇹Milano, Italy