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International COVID-19 Vaccines Safety Tracking Study (CoVaST-RU): Participation of the Russian Federation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F21%3A00124034" target="_blank" >RIV/00216224:14110/21:00124034 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.mediasphera.ru/issues/profilakticheskaya-meditsina/2021/12/1230549482021121031?clear_cache=Y" target="_blank" >https://www.mediasphera.ru/issues/profilakticheskaya-meditsina/2021/12/1230549482021121031?clear_cache=Y</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.17116/profmed20212412131" target="_blank" >10.17116/profmed20212412131</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    International COVID-19 Vaccines Safety Tracking Study (CoVaST-RU): Participation of the Russian Federation

  • Original language description

    Side effects associated with COVID-19 vaccines play a crucial role in the public decision regarding the importance and necessity of vaccination. Objective. Global active surveillance of the safety and efficacy of COVID-19 vaccines. The importance of participation of the Russian Federation is determined by obtaining data on the efficacy and safety of vaccines approved for use in the country, such as GamCOVID-Vac (Sputnik V), EpiVacCorona, CoviVac, and Sputnik Light, and comparing them with vaccines used abroad. Material and methods. The international study includes 3 phases to evaluate vaccine efficacy and safety in target populations. The first phase will study adverse reactions associated with primary vaccination, the second phase will investigate the side effects of booster doses, and the third phase will assess the long-term safety and efficacy of COVID-19 vaccines. Validated electronic questionnaires completed by the target population will be used for data collection. Expected results. The study will provide evidence-based data on the efficacy and safety of domestic vaccines in comparison with foreign vaccines. The study protocol is registered at ClinicalTrials.gov under the identifier NCT04834869. Russian Federation (CoVaST-RU) is included in the study on 26 July 2021.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    30304 - Public and environmental health

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Profilakticheskaya meditsina

  • ISSN

    2305-4948

  • e-ISSN

  • Volume of the periodical

    24

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    RU - RUSSIAN FEDERATION

  • Number of pages

    10

  • Pages from-to

    31-40

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-85128414532