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Non invasive ventilation severe respiratory failure in pneumonia

Safety and efficacy of non invasive ventilation in severe respiratory failure due to community acquired pneumonia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCH-12002124
Enrollment
Unknown
Registered
2012-04-26
Start date
2012-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Respiratory failure -pneumonia

Interventions

patient with cap:non invasive ventilation

Sponsors

Respiratory Diseases Department, General Hospital of Sestri Levante
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patient with pneumonia and severe respiratory failure (paO2/FIO2 lower than 250) without septic shock and multiorgan failure

Exclusion criteria

Exclusion criteria: patient with multiorgan failure ,septic shock and who need intubation

Design outcomes

Primary

MeasureTime frame
success of non invasive ventilation (avoid intubation);—

Countries

Italy

Contacts

Public ContactNicolini Antonello
antonello.nicolini@fastwebnet.it+39 01 85329145

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026