Infants With Severe Acute Respiratory Distress Syndrome: The Prone Trial

Recruiting N/A Interventional Study
Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS) Surfactant Dysfunction Infant
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
Up to 12 Months
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
14 (estimated)
Sponsor
Medical University of Vienna · Other
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About This Trial
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 administ…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients hospitalized at Pediatric Intensive Care Unit (PICU) or Neonatal Intensive Care Unit (NICU) of the Medical University Vienna. * Patients aged \>36 weeks (corrected gestational age) and \<24 months. * Patient intubated and mechanically ventilated for at least 6 hours, …
Contacts

Tobias Werther

+4314040032320

tobias.werther@meduniwien.ac.at

CONTACT

Michael Hermon

+4314040032320

michael.hermon@meduniwien.ac.at

CONTACT