Validation and Precision Treatment of Inflammatory Subphenotypes in Acute Respiratory Distress Syndrome: A Multicenter Cohort Study

Recruiting Observational Study
Acute Respiratory Distress Syndrome
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
500 (estimated)
Sponsor
Southeast University, China · Other
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About This Trial
Acute respiratory distress syndrome (ARDS) is a common and life-threatening condition in intensive care units, characterized by substantial biological and clinical heterogeneity. Differences in patients' inflammatory responses, baseline immune function, and organ failure patterns contribute to variability in ARDS severity, treatment response, and clinical outcomes. Precision classification of ARDS…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 18 years. 2. ARDS with new Global definition. 3. Onset of ARDS within 72 hours. Exclusion Criteria: 1. Refusal of informed consent by the patient's legally authorized representative. 2. Patients expected to die within 24 hours 3. Receiving extracorporeal membrane oxyg…
Contacts

Hui Chen, MD

+8618006138640

huichen.icu@gmail.com

CONTACT