Intubation
Conditions
Interventions
This is a randomized, controlled clinical trial. Patients will be randomized 1:1 with the aid of a randomization program. The experimental group: 50 patients with bronchopneumonia under mechanical ven
Sponsors
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients under mechanical ventilation; both genders; over 18 years old; pneumonia
Exclusion criteria
Exclusion criteria: High probability of death within 24 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in the Clinical Pulmonary Infection Score (CPIS) by 50% in 7 days. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate antibiotic use and duration;Evaluate antibiotic use and duration;Assess the length of hospital stay | — |
Countries
Brazil
Contacts
Public ContactEllen de Oliveira
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Outcome results
None listed