Stopped: Inadequate funds allocated for study completion
Feasibility study to randomize non-vigorous newborn infants born through meconium-stained amniotic fluid to endotracheal suctioning or immediate resuscitation.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Ability to identify, consent, enroll and randomize 70% of eligible infants into study.
Timeframe: 18 months
The number of infants in the study who develop meconium aspiration syndrome, require extracorporeal membrane oxygenation or die
Timeframe: 18 months