Makassed General Hospital
Beirut, Lebanon
NCT Number: NCT04397991
This is a randomized double blind clinical trial in which newborns with suspected Transient tachypnea of the newborn (TTN) will receive either furosemide or normal saline by nebulizer every 6 hours for 24 hours.
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All sexes
Interventional
Not applicable
Beirut, Lebanon
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive nebulised furosemide solution 1 mg/kg
Patients will receive nebulised 0.9% saline
Time frame: 24 hours
Neonatal respiratory morbidity will be assessed through oxygen saturation, respiratory rate and duration on Continuous positive airway pressure (CPAP)
Time frame: 15 days
Duration of hospital stay in days
Makassed General Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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