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临床试验/NCT04871789
NCT04871789Unknown不适用

Optimization of Patients Long-term Management After the Coronavirus Infection COVID-19

Pirogov Russian National Research Medical University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2021年1月20日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
200
试验地点
1
主要终点
The presense of postcovid syndrome

研究概览

简要总结

200 participants should be included in the study. There will be three groups: 100 participants with a severe course of the disease 3 months ago, 50 asymptomatic carriers of coronavirus infection 3 months ago and 50 people who were in close contact with patients with confirmed coronavirus infection 3 months ago, but not sick and without antibodies to SARS-CoV-2.

The study consists of two visits. At the first visit, after signing the consent to participate in the study, a screening examination will be performed to assess the criteria for inclusion and exclusion in the study.

At the second visit, patients who meet the inclusion criteria and do not have exclusion criteria will undergo clinical and instrumental examination, and biological samples will be collected for laboratory testing.

The aim of the study is to determine the most significant clinical and laboratory markers of the severity of the outcomes in the period of convalescence of the new coronavirus infection COVID-19. Clinical and laboratory indicators, the number and severity of signs of postcovid syndrome as well as pathological changes in lung tissue according to CT data in the group with covid pneumonia and indicators of immune status, hemostasis, endothelial dysfunction, inflammation, metabolism will be assessed.

研究设计

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

入排标准

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

入选标准

  • •For all groups:
  • •Informed consent signed by the patient.
  • •Men and women aged 18 and over.
  • •Group COVID-19 (asymptomatic):
  • •Confirmed diagnosis of COVID-19 (positive SARS-CoV-2 RNA PCR test or history of IgM and / or IgG antibodies to SARS-CoV-2)
  • •Absence of any clinical symptoms associated with coronavirus infection.
  • •Group Healthy:
  • •Contact with patients with symptomatic new coronavirus infection COVID-19 in the absence of personal protective equipment for at least 3 days.
  • •Absence of any clinical symptoms associated with coronavirus infection
  • •Group COVID symptomatic:
  • •Confirmed diagnosis of previous COVID-19 (positive SARS-CoV-2 RNA PCR test or presence of IgM antibodies to SARS-CoV-2) in history.
  • •A severe course of COVID-19, characterized by one or more of the following symptoms:
  • •Respiratory rate ≥ 30 in 1 min
  • •Blood oxygen saturation (SpO2) ≤ 93%
  • •The ratio of the partial tension of oxygen in arterial blood to the fraction of oxygen during inspiration (PaO2 / FiO2) <300
  • •Lung tissue lesion> 50% and / or according to computed tomography CT-2 and higher
  • •Septic shock / sepsis
  • •Development of multiple organ failure
  • •Cytokine storm

排除标准

  • •Pregnancy
  • •Covid-19 vaccination
  • •Any serious medical illness before coronavirus infection, as well as a permanent form of atrial fibrillation
  • •Regular intake of anti-inflammatory, antibacterial, cytostatic and immunosuppressive drugs
  • •Refusal to participate in the study

结局指标

主要结局

The presense of postcovid syndrome

时间窗: through study completion, an average of 3 months

Clinical and laboratory indicators The number and severity of signs of postcovid syndrome

次要结局

  • Pathological changes in lung tissue according to CT data(through study completion, an average of 3 months)

研究者

发起方
Pirogov Russian National Research Medical University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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