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Study identifier: NCT04777760 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Surfactant for Neonatal Respiratory Distress Syndrome(NRDS) and Neonatal Acute Respiratory Distress Syndrome(NARDS)

Condition: Respiratory Distress Syndrome · Preterm Birth · Acute Respiratory Distress Syndrome  ·  Sponsor: Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

PhaseN/A
Planned participants400
Who can joinAll sexes, 1 Minute to 24 Hours
Healthy volunteersNo

About this study

In preterm infants with neonatal respiratory distress syndrome (NRDS), exogenous pulmonary surfactant(PS) replacement therapy is one of the most important therapeutic breakthrough to reduce neonatal mortality. Nowadays, PS is commonly used in newborn infants with respiratory distress, but the incidences of bronchopulmonary dysplasia(BPD) and/or death are inconsistent. The result indicates that not all preterm infants with respiratory distress can be beneficial from PS. In 2017, the international neonatal ARDS (NARDS) collaborative group provides the first consensus definition for NARDS. And whether or not PS being beneficial for preterm infants with NARDS remains unknown.

This description comes directly from the study's public registry record.

Talk to the study team

Chen Long, MD, PhD  ·  +8613883559467  ·  neuroclong@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

ChenChongqing, Chongqing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04777760