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Assessment Of Dose-Dependent Immunomodulatory Effect Of Alveofact With or Without Steroisd In Neonatal RDS

Assessment Of Dose-Dependent Immunomodulatory Effect Of Alveofact With or Without Steroisd In Neonatal RDS

Recruiting
1-2 years
All
Phase 1

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Overview

An Exploratory Randomized double-arm controlled trial to evaluate the immunomodulatory effect of low versus high dose of Alveofact with or without Budesonide.

Description

Neonatal respiratory distress syndrome (RDS) is caused by lung immaturity and surfactant deficiency in preterm newborns and is an important cause of morbidity and mortality.

Surfactant therapy plays an essential role in the management of RDS as it reduces lung injury and improves survival, While surfactant alone is very effective, some studies showed that its combination with budesonide significantly reduces BPD and inflammatory markers.

Neutrophils extracellular traps (NETs) are a defense mechanism where neutrophils are the reaction to microbial infection and cast a net-like structure. NETs are composed of chromatin decondensed and some 30 enzymes and peptides. Many components such as Neutrophil elastase (NE) and Myeloperoxidase enzyme (MPO) have antimicrobial, but also a cytotoxic property that causes tissue injury. The immune regulatory abilities of the pulmonary surfactant are known to alter the function of the adaptive and innate immune cells.

So, in this study, The Investigator will Assess the immunomodulatory effect of low and high doses of Alveofact with or without Budesonide.

Eligibility

Inclusion Criteria:

  • Gestational age ≤ 35 weeks with
    1. Respiratory distress syndrome.
    2. Need surfactant administration based on European RDS consensus: (Sweet et al., 2019)
    3. If intubation is required as part of stabilization.
    4. Clinically presenting with increased work of breathing including (tachypnea, nasal flaring, grunting, retractions, and cyanosis, with decreased air entry on auscultation.
    5. Babies who are worsening when FiO2 >0.30 on CPAP pressure of at least 6 cm H2O to maintain normal saturations.

Exclusion Criteria:

Preterm neonates with evidence of any of the following will be excluded:

  1. Chromosomal anomaly or Congenital heart defect
  2. Hemodynamically significant patent ductus arteriosus.
  3. Early-onset sepsis or bacterial infection
  4. Congenital pneumonia
  5. Intra ventricular hemorrhage (IVH)
  6. Parenteral refusal to participate.

Study details
    Neonatal Respiratory Distress Syndrome
    Inflammatory Response
    Premature Lungs
    Neutrophil Extracellular Trap Formation
    Preterm Birth

NCT06367881

Ain Shams University

4 May 2024

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