Acute Respiratory Distress Syndrome Clinical Trial
Official title:
Phase II, Randomized, Placebo-Controlled, Double-Blind Clinical Trial to Evaluate the Effects and Safety of Infusion of Low-Doses of Methylprednisolone in Early ALI and ARDS in Children
The purpose of this study is to investigate the effects of prolonged low-dose methylprednisolone infusion on pulmonary function (LIS and ventilation-free days), extra pulmonary organ function (PMODS score), inflammatory markers - RCP (Reactive C Protein), IL6 (Interleukine 6), TNFα (Tumor Necrosis Factor), IL8 (Interleukine 8), IL10 (Interleukine 10) and length of Pediatric Intensive Care Unit (PICU) stay in early ALI/ARDS in children.
Scientific background. Dysregulated systemic inflammation - characterized by protracted
elevation of inflammatory cytokines in the circulation - is a key pathogenetic mechanism for
morbidity and mortality in ALI/ARDS, and is associated with tissue insensitivity and/or
resistance to inappropriately elevated endogenous glucocorticoids. In one study, prolonged
methylprednisolone treatment of ARDS patients resulted in rapid and sustained reduction in
circulating and pulmonary levels of pro-inflammatory cytokines, chemokines, and procollagen.
Preliminary work. Two recent metanalysis evaluating the use of low doses of corticosteroids
in acute lung injury/ARDS in adults reported a significant physiological improvement, a
sizable reduction in duration of mechanical ventilation and ICU length of stay and reduction
in mortality.
Hypothesis. We hypothesized that prolonged administration of low doses of methylprednisolone
in pediatric ALI/ARDS is safe and downregulates systemic inflammation and leads to earlier
resolution of pulmonary and extra pulmonary organ dysfunction and a reduction in duration of
mechanical ventilation and ICU stay.
Objective. To investigate the effects of prolonged low-dose methylprednisolone infusion on
pulmonary function (LIS and ventilation-free days), extra pulmonary organ function (PMODS
score), inflammatory markers - RCP (Reactive C Protein), IL6 (Interleukine 6), TNFα (Tumor
Necrosis Factor), IL8 (Interleukine 8), IL10 (Interleukine 10) and length of Pediatric
Intensive Care Unit (PICU) stay in early ALI/ARDS in children.
Study design. Prospective randomized, placebo-controlled, double-blind clinical trial.
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