MINImising Total Radiation EXposure in Preterm Infants

Recruiting Phase 2 Interventional Study
Neonatal Respiratory Distress Syndrome PreTerm Neonate
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
Up to 24 Hours
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Diagnostic
Participants needed
180 (estimated)
Sponsor
Western Health, Australia · Government
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About This Trial
Being born too early (preterm birth) is the leading cause of death in children world-wide. In Australia, 97% of very preterm babies who are admitted to Neonatal Intensive Care Units need breathing support after birth to survive. Despite this significant global impact, neonatal clinicians have few tools available to guide breathing support. Currently, the only lung imaging tool that is routinely us…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: All infants born \<32 weeks' gestation and admitted to the neonatal intensive care unit (NICU) who require lung imaging for respiratory indications will be considered eligible. Each infant must meet all the following criteria to be enrolled in this study: * The infant is born f…
Contacts

Arun Sett, PhD

+61405491595

Arun.Sett@wh.org.au

CONTACT

Niranjan Abraham, MD

0413751479

Niranjan.AbrahamWilliam@wh.org.au

CONTACT