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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
GroupInterventionDescription
NIVNon-invasive ventilationAll patients with acute respiratory failure treated with non-invasive ventilation who give informed consent about treatment of their clinical data
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod

Trial Locations

Locations (1)

Ospedale San Raffaele di Milano

🇮🇹

Milano, Italy

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