Outcome of Extremely Preterm Infants Who Received Systemic Postnatal Corticosteroid for Bronchopulmonary Dysplasia - Trial NCT05055193
Access comprehensive clinical trial information for NCT05055193 through Pure Global AI's free database. This phase not specified trial is sponsored by Hospices Civils de Lyon and is currently Completed. The study focuses on Bronchopulmonary Dysplasia. Target enrollment is 400 participants.
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Study Focus
Evaluation at 24 months corrected age: respiratory outcome, Neurodevelopmental outcome, Growth outcome
Observational
drug
Sponsor & Location
Hospices Civils de Lyon
Timeline & Enrollment
N/A
Jan 01, 2013
Dec 31, 2018
Primary Outcome
Composite primary outcome combining: - Respiratory evolution at 24 months corrected age - Neurodevelopmental evolution at 24 months corrected age - Growth evolution at 24 months corrected age
Summary
Bronchopulmonary dysplasia is a complication of prematurity. Postnatal corticosteroid is used
 to treat the inflammatory part of this pathology, in particular to wean premature infants
 from the ventilator at the end of the first month of life. However, this therapy remains
 controversial because it may induce suboptimal neurocognitive development. Parents of infants
 who receive postnatal corticosteroid should be provided with information about the risks. The
 objective of our work was to evaluate the respiratory, neurodevelopmental and growth outcomes
 at 24 months corrected age of extremely preterm infants who received postnatal
 corticosteroid.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05055193
Non-Device Trial