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NCT07675265
Observational, Non-interventional Biomarker and Endotyping Study
Conditions: ARDS (Acute Respiratory Distress Syndrome)
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 1200
Sponsor: Prenosis, Inc.
Summary
The goal of this observational study is to establish a centralized ARDS biorepository of longitudinal biospecimens and harmonized clinical data, develop unsupervised, therapy-agnostic endotyping algorithms, and develop unsupervised, therapy-specific treatment-prediction algorithms over a 24 month period.
Eligibility Criteria
Inclusion Criteria:
* Age ≥18 years
* ARDS Diagnosis (New Global Definition of ARDS)
* Timing: Acute onset within 7 days
* Radiology: Bilateral pulmonary opacities
* Hypoxia:
Non-intubated ARDS: PaO2:FIO2\
Source: ClinicalTrials.gov (NCT07675265). StuddyBuddy aggregates publicly available trial information.
