Medical-biological Research of the Pathogenesis of COVID-19 Disease Caused by SARS-CoV-2
NCT ID: NCT04611841
Last Updated: 2020-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
250 participants
OBSERVATIONAL
2020-07-21
2022-12-31
Brief Summary
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Detailed Description
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A comprehensive assessment of the biological parameters of the virus and the parameters of the immune response to infection is required. In this regard, we propose an integrated approach, including the use of PCR testing technology, analysis of the immune response in the form of antibodies of all major classes (IgG, IgA), determination of inflammation markers, C-reactive protein, detailed blood test, ferritin and troponin.
In addition, an analysis of the genetic diversity of strains of the pathogen COVID-19 circulating among various groups of the population of the Russian Federation will be carried out.
To collect and analyze data, it is planned to enter information into a special electronic system and analyze the collected data with a wide range of informative methods that allow "layer by layer" to compare and collect a complete picture of what is happening.
Objectives of the study:
1. Identifying the percentage of infected in the population in Moscow, the Moscow region and some other regions where the epidemic situation in connection with SARS-CoV-2 remains tense;
2. Study of genetic diversity (including metavirome) and dynamics of structural variability of the causative agent of coronavirus infection in the studied regions;
3. Studying the features of the formation and tension of immunity in patients who have undergone coronavirus infection of varying severity;
4. Clarification of the mechanisms of occurrence and development of coronavirus infection.
In the study of biological samples obtained from research participants, methods of proteomics, peptidomics, next generation sequencing (NGS), physicochemical methods of analysis will be used.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* COVID-19 diagnosis confirmed by PCR test
* Written consent to participate in the study
Exclusion Criteria
* A serious condition with a threat to life or contraindications that prevent the collection of biomaterial
* Oncological diseases outside the stage of remission
18 Years
75 Years
ALL
No
Sponsors
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Burnasyan Federal Medical Biophysical Center
OTHER_GOV
Federal Research Clinical Center of Federal Medical & Biological Agency, Russia
OTHER_GOV
Moscow city hospital named after S.I. Spasokukotskiy
UNKNOWN
Federal State Public Scientific Institution, Scientific Center for Family Health and Human Reproduction Problems
OTHER
Federal State Budgetary Healthcare Institution, Hospital RAS
UNKNOWN
Federal Research and Clinical Center of Physical-Chemical Medicine
OTHER
Responsible Party
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Principal Investigators
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Vadim Govorun, MD
Role: STUDY_DIRECTOR
FRCC PCM
Locations
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Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency
Moscow, , Russia
Countries
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Other Identifiers
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COV2020
Identifier Type: -
Identifier Source: org_study_id