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A study of lung infections in patients with acute respiratory distress syndrome on ventilator.

Clinical and microbiological profile of ventilator associated pneumonia in patients with acute respiratory distress syndrome (ARDS) requiring invasive mechanical ventilation. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/05/111393
Enrollment
141
Registered
2026-05-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: J80- Acute respiratory distress syndrome

Interventions

Intervention1: Nil: Nil

Sponsors

Vivekananda Pingali
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults (equal to or greater than 18 years) admitted to the intensive care unit (ICU) with a diagnosis of ARDS according to the updated global ARDS definition. Patients requiring invasive mechanical ventilation for at least 48 hours to ensure the development of VAP is accurately assessed.

Exclusion criteria

Exclusion criteria: Patients less than 18 year of age ARDS without invasive mechanical ventilation Intubated from outside for more than 24 hours. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of ventilator associated pneumoniaTimepoint: Baseline, weekly, time of discharge, 28 days.

Secondary

MeasureTime frame
In Hospital and ICU mortalityTimepoint: ;28 day survivalTimepoint: 28 days;length of icu stayTimepoint: ;duration of ventilator free dayTimepoint:

Countries

India

Contacts

Public ContactVivekananda Pingali

Kasturba Medical College, Manipal

shubhada.u@manipal.edu

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026