CTRI/2024/01/061829Not yet recruitingUnknown
Development of screening tool to identify fatal hyperinflammatory subphenotype-2 of acute respiratory distress syndrome (ARDS) with Point-of-Care Ultrasound, ventilatory mechanical power, and blood cell count-derived biomarkers. - Nil
SHWETHAPRIYA R0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
Inclusion Criteria
- •Adult ARDS patients as per Berlin criteria
Exclusion Criteria
- •Patients with ARDS diagnosis > 24 hours.
- •Patients of ARDS, not on IMV.
- •Lung trauma, chest wall deformities where POCUS may be unreliable.
- •Previously known causes of right ventricular dysfunction.
- •Patients on previous corticosteroids where NLR, SIII ratio will be unreliable.
- •Patients with known CKD where Renal arterial Resistive Index (RII) will be unreliable.
Investigators
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