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Clinical Trial Summary

Feasibility study to randomize non-vigorous newborn infants born through meconium-stained amniotic fluid to endotracheal suctioning or immediate resuscitation.


Clinical Trial Description

This will be a pilot feasibility trial of endotracheal intubation and suctioning versus routine resuscitation for term, non-vigorous newborns born through meconium-stained amniotic fluid to compare the incidence of meconium aspiration syndrome, extracorporeal membrane oxygenation or death. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02708563
Study type Interventional
Source St. Louis University
Contact
Status Withdrawn
Phase N/A
Start date July 2019
Completion date July 2021

See also
  Status Clinical Trial Phase
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Not yet recruiting NCT02571231 - High Flow Ventilation With Volume Guarantee N/A
Completed NCT01758822 - Role of Endotracheal Suction on the Occurrence of Meconium Aspiration Syndrome in Non-vigorous Meconium Stained Babies N/A
Completed NCT01328483 - Effect Of Intrapartum Oropharyngeal (IP-OP) Suction on Meconium Aspiration Syndrome N/A
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Recruiting NCT03346343 - Pulmonary Function Using Non-invasive Forced Oscillometry N/A
Completed NCT01757782 - Oral Sildenafil in Persistent Pulmonary Hypertension Secondary to Meconium Aspiration Syndrome in Newborns Phase 4
Completed NCT01274845 - Use of Heliox in the Management of Neonates With Meconium Aspiration Syndrome N/A
Recruiting NCT00312507 - Surfactant Lavage vs. Bolus Surfactant in Neonates With Meconium Aspiration Phase 3