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An observational study on Acute Respiratory Distress Syndrome (ARDS) in India

Snap shot of Acute Respiratory Distress Syndrome (ARDS) in India

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2014/08/004880
Enrollment
300
Registered
2014-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Acute Respiratory distress Syndrome

Interventions

None listed

Sponsors

Fulbright Scholarship
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.- Patients who are admitted to the ICU and are diagnosed with ARDS using Berlin criteria 2.- Patients who are admitted to the ICU with a diagnosis of ARDS will be included weather they are managed with invasive or non invasive ventilation. We suspect it will be a rare patient that can be managed by non invasive ventilation. 3.- This study will be conducted in Intensive Care Units (MICU, CCU, SICU, etc) that are willing to participate in the study. There will be one site principal investigator who will be responsible for entering the data on all the ICUs in a hospital. 4.- Patients in whom mechanical ventilation was started outside the study ICU at the same Institution and/or a different Institution, including Emergency Room, Operating Room (OR), and were then transferred to the ICU with the diagnosis of ARDS are also included.

Exclusion criteria

Exclusion criteria: 1.- The following ICUs will be excluded: a) Pediatric ICU b) Post-op Anesthesia Recovery Room 2.- Patient less than 18 yr

Design outcomes

Primary

MeasureTime frame
Discharge from the ICU and/or deathTimepoint: 24 hours after successful extubation and 28 days after enrollment in the study

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Kalpalatha Guntupalli

Pulmonary Critical Care and Sleep

guntupalli00@gmail.com

Outcome results

None listed

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