Skip to content

Improving Non-invasive Ventilation

Improving Non Invasive Ventilation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01571986
Acronym
Improving NIV
Enrollment
750
Registered
2012-04-05
Start date
2012-02-29
Completion date
2026-05-31
Last updated
2025-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Failure

Keywords

NIV, acute respiratory failure, hypoxia, hypercapnia, non-invasive ventilation, hospital ward

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.

Interventions

PROCEDURENon-invasive ventilation

Non-invasive ventilation

Sponsors

Università Vita-Salute San Raffaele
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* treatment with non-invasive ventilation * informed consent

Exclusion criteria

* refusal of informed consent

Design outcomes

Primary

MeasureTime frame
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.

Countries

Italy

Contacts

Primary ContactLuca Cabrini, MD
cabrini.luca@hsr.it

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026