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Predicting outcomes in patients at risk for acute respiratory distress using right heart function status.

Prevalence of Right Ventricular dysfunction subphenotypes and their utility as predictor of outcomes in patients of ARFA (At risk for ARDS) on invasive mechanical ventilation - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096341
Enrollment
174
Registered
2025-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: J988- Other specified respiratory disorders

Interventions

Intervention1: Nil: Nil

Sponsors

JERUSHA MATHEWS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients more than 18 years on invasive mechanical ventilation admitted in Kasturba hospital Patients in ARFA (i.e., not entirely fulfilling the diagnostic criteria of ARDS) Presence of any of the following radiological features(C-X-ray, Lung ultrasound,CT) 1.Alveolar infiltrates (can be hemorrhagic) 2.Interstitial infiltrates 3. Atelectasis 4.Consolidation 5.Ground glass opacities 6.Air bronchogram in lung ultrasound Respiratory Symptoms (at least one) New or increased cough New or increased sputum production Dyspnea Pleuritic chest pain Other Signs or Findings (at least one) Abnormal lung sounds (rhonchi or rales) Fever (more than or equal to 100.4 °F) Leukocytosis or unexplained bandemia (above normal limits for laboratory) Hypoxia (less than 90%)

Exclusion criteria

Exclusion criteria: 1)ARFA patients on NIV 2)Patients not recruited within first 24 hours of IMV 3)Patients already having pre-existing Pulmonary Artery Hypertension 4)Patients having pre-existing EF of less than 40 per cent 5)Patients on any biological agent, prednisone equivalent of more than 10 mg per day and 700 mg cumulative dose , antiproliferative agents and B or T cell depletion medications 6)Patients having malignancies

Design outcomes

Secondary

MeasureTime frame
nilTimepoint: nil

Primary

MeasureTime frame
Demographic , biochemical and Echo/USG data will be collected within 72 hours of admission which is part of standard of care. Hence the investigator will only collect the reports. Outcome will assessed based on duration of Icu stay, use of vasopressors and mechanical ventilation. Outcomes will be analyzed at the time of discharge – Improved/ExpiredTimepoint: 24 HOURS , 72 HOURS

Countries

India

Contacts

Public ContactVASUDEVA ACHARYA

KASTURBA MEDICAL COLLEGE , MANIPAL

acharya.vasudeva@manipal.edu9740225485

Outcome results

None listed

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