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Clinical Trial Summary

A comprehensive strategy will be used to investigate the relationship and correlation between 4 diagnostically significant markers relevant for early diagnosis and prediction of complications and death in the development of sepsis in children (C-reactive protein, procalcitonin, presepsin and lipopolysaccharide binding protein). For the first time, an attempt will be made to assess the genetic characteristics of the patient's from the point of view of predisposition to the unfavorable development of the sepsis based on the study of polymorphism of a number of genes of the immune system (tumor necrosis factor beta; interleukin 6, 8, 10; lymphotoxin alpha, etc.). Based on the study results, an algorithm to predict the unfavorable course of sepsis in children will be developed using a comprehensive assessment of biochemical and molecular genetic markers.


Clinical Trial Description

- analyze biochemical markers and immune status data in sepsis patients and in the comparison group; - assess the state of the cellular immunity, level of pro-inflammatory cytokines, genetic polymorphism of immune response genes in sepsis patients; - carry out a correlation analysis of clinical and laboratory data and immune system among patients of different groups (with and without septic shock, taking into account the outcome); - assess the relationship between the genetic characteristics of the patient's immune system and the severity of the pathological process; - based on the data obtained, prepare instructions for use, which describes an algorithm to predict the unfavorable course of sepsis in children. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05908162
Study type Observational
Source The Republican Research and Practical Center for Epidemiology and Microbiology
Contact Oksana N Romanova, Dr
Phone +375172022505
Email romox@tut.by
Status Recruiting
Phase
Start date July 1, 2021
Completion date July 1, 2024

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