High Flow Nasal Cannula Versus Bubble Nasal CPAP for the Treatment of Transient Tachypnea of the Newborn in Infants ≥ 35 Weeks Gestation
Stopped early · Not applicable
Conditions studied: Transient Tachypnea of the Newborn
In brief
The primary objective is to determine whether High Flow Nasal Cannula (HFNC) is a superior respiratory modality for neonates ≥36 weeks with transient tachypnea of the newborn (TTN) when compared to the standard of care modality (NCPAP).
Key facts
- Study ID
- NCT01270581
- Run by
- Icahn School of Medicine at Mount Sinai
- People needed
- 7
- Starts
- 2010-07-01
- Expected to finish
- 2012-04-01
- Last updated by the study team
- 2017-02-16
Who can join
Age: any, up to 0. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- gestational age ≥ 35 weeks
- diagnosis of TTN, defined as respiratory rate >60, presence of subcostal and /or intercostal retractions, nasal flaring, grunting, oxygen saturations 70-93% on room air, and radiological evidence of perihilar streaking and patchy infiltrates
- admission to the NICU at Mount Sinai hospital within first 24 hours of life
You may not qualify if…
- gestational age < 35 weeks
- history of thick meconium stained fluid and/or diagnosis of meconium aspiration syndrome
- diagnosis of major congenital pulmonary or cardiac anomalies
- initial CXR demonstrating air leak
- respiratory distress first occurring after 24 hours of life
- presumptive diagnosis of RDS as indicated by the need for FiO2 > 40%, severe retractions and grunting with poor air entry, and diffuse alveolar consolidation on chest radiograph
Where it is running
- Mount Sinai School of Medicine — New York, New York, United States
Full record on ClinicalTrials.gov
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