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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04777760
Other study ID # surfactant for NRDS and ARDS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date December 31, 2024

Study information

Verified date October 2022
Source Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Contact Chen Long, MD, PhD
Phone +8613883559467
Email neuroclong@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In preterm infants with neonatal respiratory distress syndrome (NRDS), exogenous pulmonary surfactant(PS) replacement therapy is one of the most important therapeutic breakthrough to reduce neonatal mortality. Nowadays, PS is commonly used in newborn infants with respiratory distress, but the incidences of bronchopulmonary dysplasia(BPD) and/or death are inconsistent. The result indicates that not all preterm infants with respiratory distress can be beneficial from PS. In 2017, the international neonatal ARDS (NARDS) collaborative group provides the first consensus definition for NARDS. And whether or not PS being beneficial for preterm infants with NARDS remains unknown.


Description:

To date, PS is not recommended to adult and pediatric ARDS. Meantime, systematic review indicates that PS does not demonstrate statistically significant beneficial effects on reducing the mortality and the rate of BPD in term and late preterm infants with meconium aspiration syndrome(MAS). Therefore, a reasonable speculation is that preterm infants with NARDS do not benefit from one dose of PS. And the speculation can explain why not all preterm infants with respiratory distress can be beneficial from PS. In the era of pre-NARDS, the preterm infants fulfilling the definition of NARDS may have been considered as NRDS in the first three days after birth. According to the diagnostic criteria of NARDS, a key procedure for diagnosis of NARDS is to exclude the newborn infants with NRDS. But no detailed procedures are available to differentiate NRDS from NARDS.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers
Gender All
Age group 1 Minute to 24 Hours
Eligibility Inclusion Criteria: Eligibility requirements for neonates were as follows: - The gestational age is less than 37 weeks and admitted to neonatal intensive care unit(NICU) in 24 h after birth - The neonates will be diagnosed with NRDS or NARDS - The neonates will be at least administrated one dose of surfactant Exclusion Criteria: one of the following criteria will be needed - major congenital anomalies - chromosomal abnormalities - upper respiratory tract abnormalities

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
one dose of surfactant replacement
the preterm infants diagnosed with NRDS and/or NARDS will be administrated with only one dose of surfactant
two and more doses of surfactant replacement
the preterm infants diagnosed with NRDS and/or NARDS will be administrated with two and more doses of surfactant

Locations

Country Name City State
China Chen Chongqing Chongqing

Sponsors (2)

Lead Sponsor Collaborator
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University Children's Hospital of Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary bronchopulmonary dysplasia(BPD) the preterm infants will be diagnosed with BPD at 36 weeks' gestational age or before discharge from hospital
Primary death the preterm infants die at 36 weeks' gestational age or before discharge from hospital
Primary BPD and/or death the preterm infants will be diagnosed with BPD and/or death at 36 weeks' gestational age or before discharge from hospital
Primary the predictive powers of one dose of surfactant to diagnose NRDS the sensitivity and accuracy of one dose of surfactant to diagnose NRDS seven days after birth
Primary the predictive powers of two and more doses of surfactant to diagnose NARDS the sensitivity and accuracy of two and more doses of surfactant to diagnose NARDS seven days after birth
Secondary intraventricular hemorrhage(IVH) the preterm infants will be diagnosed with IVH before discharge or 36 weeks' gestational age
Secondary air leak the preterm infants will be diagnosed with air leak at 36 weeks' gestational age or before discharge from hospital
Secondary periventricular leukomalacia(PVL) the preterm infants will be diagnosed with PVL at 36 weeks' gestational age or before discharge from hospital
Secondary necrotizing enterocolitis(NEC) the preterm infants will be diagnosed with NEC at 36 weeks' gestational age or before discharge from hospital
Secondary patent ductus arteriosis(PDA) the preterm infants will be diagnosed with PDA at 36 weeks' gestational age or before discharge from hospital
Secondary late-onset sepsis(LOS) the preterm infants will be diagnosed with LOS at 36 weeks' gestational age or before discharge from hospital
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