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临床试验/NCT04887142
NCT04887142已完成不适用

Biochemical, Inflammatory and Genetic Factors in Patients With COVID-19

Zeljko Mijailovic10 个研究点 分布在 5 个国家目标入组 818 人开始时间: 2020年4月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
818
试验地点
10
主要终点
Number of Participants with Fatal Outcome

研究概览

简要总结

The primary goal of the VIRIONUM project is to analyze the association of clinical, socio-demographic characteristics of patients and their genetic polymorphism, inflammatory and other biochemical markers with disease progression and death in subjects with COVID-19 disease. The research is an observational, cohort study with nested-case control design, including adult, male and female COVID-19 inpatients. Primary dependent variable will be outcome of disease, defined as discharge from the hospital or death. The outcomes and putative risk factors will be analyzed using binary logistic regressions. The proposed multi- and inter-disciplinary study should provide additional scientific evidence about risk factors for the development of severe forms of the disease and the COVID-19-related death.

详细描述

Background: Severe acute respiratory syndrome 2 (SARS-CoV-2) is etiological agent of heterogeneous corona-virus disease 19 (COVID-19), which clinical condition range from asymptomatic or mild to critically severe with high odds for fatal outcome. Since the pathophysiological pathways of COVID-19 disease development are not fully elucidated, resulting in repeated changes in treatment plans, there is an unmet need for more research into genetic, biochemical, immunological, and clinical predictive indicators of better outcomes in COVID-19 patients.

Aim: The VIRIONUM project's main aim is to investigate the relation between genetic polymorphisms, inflammatory and other biochemical markers, and disease severity and mortality in COVID-19-infected hospitalized patients.

Method and patients: The observational nested case-control clinical study will be conducted in at least 1019 COVID-19 patients. The genetic polymorphisms (ACE2, IFNL3/4 and TMPRSS2), serum concentration of soluble ACE2 and the pro- and anti-inflammatory cytokines, blood concentration of common inflammatory and other biomarkers, peripheral blood mononuclear leukocyte (PBMC) phenotype, demographic and clinical risk factors will be monitored as independent variables, while the dependent variables will be the outcome of the disease and the severity of the clinical condition. Genotyping will be performed by Real-Time PCR method, and serum concentrations of ACE2 and pro- and anti-inflammatory cytokines by ELISA method, and PBMC phenotype by flow cytometry. The disease severity will be assessed according to WHO criteria.

Expected results: The findings of this clinical study will contribute to understanding of significant genetic, biochemical, and clinical determinants of severity and lethal outcomes in COVID-19 patients, as well as, creation of set of recommendations for individuals at higher risk - future, evidence-based, targeted and individualized approach.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult age, 18 years old or more
  • Male or female
  • Hospitalization for COVID-19 after confirmation by SARS-CoV-2 rapid antigen test or RT-PCR
  • Voluntary written consent of the subject to participate

排除标准

  • Pregnant and breastfeeding women
  • Fatal outcome during the first 24 hours of hospitalization
  • Inability to collect the necessary study data
  • Declining of the subject to voluntary participate in the study

研究组 & 干预措施

The discharged subjects

The COVID-19 inpatients treated with standard care who survived the disease and discharged from hospital.

干预措施: Standard of health care (Other)

The deceased subjects

The COVID-19 inpatients treated with standard care who died from the disease.

干预措施: Standard of health care (Other)

结局指标

主要结局

Number of Participants with Fatal Outcome

时间窗: Up to 6 weeks from recruitment to hospital discharge or death

Case fatality ratio will be calculated as the proportion of patients who died from all causes (all-cause mortality) compared to the total number of patients

次要结局

  • Ordinal Scale for Clinical Improvement(Up to 6 weeks from recruitment to hospital discharge or death)

研究者

申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zeljko Mijailovic

Principal Investigator

University of Kragujevac

研究点 (10)

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