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NCT05451342

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

Status unknown Last updated 11 July 2022
What this trial tests

trial testing Integrated Transcriptomics, Metabolomics, and Lipidomics Profiling in Acute Respiratory Distress Syndrome in 200 participants. Status unknown.

Timeline
15 February 2022
Primary endpoint
15 February 2024
15 June 2024

Quick facts

Lead sponsorPeking Union Medical College Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment200
Start date15 February 2022
Primary completion15 February 2024
Estimated completion15 June 2024
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

18 and older, any sex, with Acute Respiratory Distress Syndrome or Acute Respiratory Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

6 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Clinical applications of stem cell-derived exosomes.
    Tan F, Li X, Wang Z, Li J, et al · · 2024 · cited 390× · PMID 38212307 · DOI 10.1038/s41392-023-01704-0
  2. Exosomes─Nature's Lipid Nanoparticles, a Rising Star in Drug Delivery and Diagnostics.
    Tenchov R, Sasso JM, Wang X, Liaw WS, et al · · 2022 · cited 336× · PMID 36354238 · DOI 10.1021/acsnano.2c08774
  3. A critical systematic review of extracellular vesicle clinical trials.
    Mizenko RR, Feaver M, Bozkurt BT, Lowe N, et al · · 2024 · cited 66× · PMID 39330928 · DOI 10.1002/jev2.12510
  4. Advancements in extracellular vesicles biomanufacturing: a comprehensive overview of large-scale production and clinical research.
    Li Z, Yan J, Li X, Chen H, et al · · 2025 · cited 7× · PMID 40046812 · DOI 10.3389/fbioe.2025.1487627
  5. Potential of extracellular vesicles for early prediction of severity and potential risk stratification in critical inflammatory diseases.
    Deng Y, Zou Y, Song X, Jiang A, et al · · 2023 · cited 3× · PMID 37195382 · DOI 10.1007/s12079-023-00763-w
  6. Effect Analysis of Extracellular Vesicles in the Treatment of Bronchopulmonary Dysplasia via Different Drug Delivery and Administration Routes.
    Xu W, Chen S, Liang T, Kang L, et al · · 2025 · PMID 41019235 · DOI 10.2147/ijn.s530819

Verify or expand the search:

Other recruiting trials for Acute Respiratory Distress Syndrome

Currently open trials in the same condition.

Other Peking Union Medical College Hospital trials

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