Viewing Study NCT04775459



Ignite Creation Date: 2024-05-06 @ 3:51 PM
Last Modification Date: 2024-10-26 @ 1:58 PM
Study NCT ID: NCT04775459
Status: COMPLETED
Last Update Posted: 2024-06-21
First Post: 2021-02-25

Brief Title: Surfactant Replacement Guided by Early Lung Ultrasound Score in Preterm Newborns With Respiratory Distress Syndrome
Sponsor: Centre Hospitalier Universitaire de Saint Etienne
Organization: Centre Hospitalier Universitaire de Saint Etienne

Study Overview

Official Title: Surfactant Replacement Guided by Early Lung Ultrasound Score LUS in Preterm Newborns 33 Weeks With Respiratory Distress Syndrome in the Neonatal Intensive Care Unit of Saint-Etienne
Status: COMPLETED
Status Verified Date: 2024-06
Last Known Status: Not yet recruiting
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ECHOSURF
Brief Summary: Lung immaturity is a major issue in neonatal unitThe surfactant administration improves the pulmonary prognosis in premature infants with hyaline membrane disease who escape continuous positive airway pressure CPAP

This surfactant had been administered at 5h25min of life in Saint Etienne from 2016 to 2019

Studies suggest that the earlier the surfactant is administered the more it can reduce the rate of bronchodysplasia and mortality And some studies show a pulmonary ultrasound could help to administrate the surfactant earlier This is why a new faster strategy for diagnosing preterms needing surfactant will be usefulness and have been done in Saint-Etienne since 2021 thanks to a ultrasound score LUS
Detailed Description: This current study analyzes the impact of early Lungs Ultrasounds which use a semi-quantitative assessment the Lung Ultrasound Score LUS in preterms 33 weeks on the time to surfactant administration

The current hypothesis is that Lung Ultrasound can increase the number of preterms with surfactant replacement within the first 3 hours of life

This is a prospective comparative observational trial between two different cohorts the last 6 months of 2019 without Score LUS versus the first 6 months of 2021 with Score LUS

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None