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NCT03311165

Epidemiological Study of Neonatal Acute Respiratory Distress Syndrome (ARDS)

Completed Last updated 9 January 2020
What this trial tests

trial testing no intervention in Neonatal Acute Respiratory Distress Syndrome(ARDS) in 1,000 participants. Completed in 30 June 2019.

Timeline
1 January 2018
Primary endpoint
30 June 2019
30 June 2019

Quick facts

Lead sponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,000
Start date1 January 2018
Primary completion30 June 2019
Estimated completion30 June 2019
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

Who can join

Adults 1 Minute to 1 Month, any sex, with Neonatal Acute Respiratory Distress Syndrome(ARDS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Neonatal acute respiratory distress syndrome(ARDS) is a rare but often severe respiratory disorder. The incidence remains unclear and mortality is about 30%-60%. It is characterized by acute, refractory hypoxemia, persistent respiratory distress and decreased lung compliance. Evaluation and comparison of various clinical studies conducted were hindered by a lack of uniformity in diagnostic criteria.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Clinical characteristics and outcomes in neonates with perinatal acute respiratory distress syndrome in China: A national, multicentre, cross-sectional study.
    Chen L, Li J, Shi Y, Chinese Neonatal ARDS (ChiNARDS) study group. · · 2023 · cited 23× · PMID 36386029 · DOI 10.1016/j.eclinm.2022.101739

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