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Explore Potential Plasma and BALF Immunometabolic and Lipidomic Biomarkers for Identifying ARDS Endotypes

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Enrolling

Conditions

Acute Respiratory Distress Syndrome
Acute Respiratory Failure

Treatments

Diagnostic Test: Integrated Transcriptomics, Metabolomics, and Lipidomics Profiling

Study type

Observational

Funder types

Other

Identifiers

NCT05451342
ZS-3391

Details and patient eligibility

About

Acute respiratory distress syndrome (ARDS) is a life-threatening condition that causes high mortality (41% to 58%). Previous studies have reported that biomarkers can facilitate phenotypic diagnosis of ARDS, enabling precision treatment of ARDS. Although there were many studies that found some potential therapeutic targets for ARDS, no pharmacotherapies have been validated to treat ARDS. The development of biomarkers to predict the prognosis and monitor the response to treatment would be of interest for selecting patients for specific therapeutic trials. Many recent studies have shown that immune metabolic changes are involved in the pathogenesis of ARDS and may become a new therapeutic target for them. We aimed to identify a panel of immunometabolic and lipidomic biomarkers derived from blood and bronchoalveolar lavage fluid (BALF) which may help differentiate the ARDS endotypes.

Full description

PROTOCOL OUTLINE:

This is an observational study. The blood and BALF samples will be collected from patients with ARDS for exosome extraction and transcriptome and metabolomic analysis.

Exosome characterization and differential genes and metabolites will be identified.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Aged >18 years old;
  2. Meet the diagnostic criteria of ARDS according to the Berlin Criteria.

Exclusion criteria

  1. Aged≤18 years old;
  2. Pregnancy;
  3. No informed consent;

Trial design

200 participants in 2 patient groups

ARDS
Description:
Patients who meet the diagnostic criteria of ARDS
Treatment:
Diagnostic Test: Integrated Transcriptomics, Metabolomics, and Lipidomics Profiling
Non-ARDS
Description:
Patients without ARDS
Treatment:
Diagnostic Test: Integrated Transcriptomics, Metabolomics, and Lipidomics Profiling

Trial contacts and locations

2

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Central trial contact

Yingying Yang, MD

Data sourced from clinicaltrials.gov

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