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Study identifier: NCT05002478 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Infants with Severe Acute Respiratory Distress Syndrome: the Prone Trial

Condition: Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS) · Surfactant Dysfunction · Infant  ·  Sponsor: Medical University of Vienna

PhaseNA
Planned participants14
Who can joinAll sexes, N/A to 12 Months
Healthy volunteersNo

About this study

The main objective is to determine the short-term effect of prone positioning in infants with infection-associated severe acute respiratory distress syndrome. The investigators compare oxygenation parameters and measurements from electrical impedance tomography (EIT) and lung ultrasonography (LUS) in mechanically ventilated infants in prone position versus supine position after surfactant administration.

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

Talk to the study team

Tobias Werther  ·  +4314040032320  ·  tobias.werther@meduniwien.ac.at

Michael Hermon  ·  +4314040032320  ·  michael.hermon@meduniwien.ac.at

Always discuss trial participation with your own doctor first.

Locations (1)

Medical University of ViennaVienna, AustriaRecruiting

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Source record: clinicaltrials.gov/study/NCT05002478