Seroprevalence of the Anti-SARS-CoV-2 Antibodies (Causing COVID-19) in Kidney Transplant Recipients in Severely Affected Region
NCT ID: NCT04874740
Last Updated: 2022-12-07
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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COMPLETED
300 participants
OBSERVATIONAL
2021-04-30
2022-10-30
Brief Summary
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Detailed Description
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The SARS-CoV-2 virus can be detected in the body by several ways. The presence of the virus can be directly confirmed by RT-PCR or by determination of viral antigen from a swab from the nasopharynx, throat, direct examination of sputum or aspirate from bronchoscopy, or rectum. Indirect methods of virus detection include the determination of antibodies in the blood. Antibodies can target several structures of the virus: spike protein (S), envelope, membrane or nucleocapsid (NP). The S protein is composed of S1 and S2 subunit. The S1 subunit contains receptor-binding domain (RBD) which is necessary for interaction and entering human cells. In practice, IgG, IgM and IgA antibodies against RBD and NP are usually detected.2,3 With regard of serious development of the COVID 19 epidemic situation in the Czech Republic, we decided to do this prevalence study. Our goal is to evaluate the seroprevalence of anti-SARS-CoV-2 antibodies in patients after kidney transplantation which is also important for possible future epidemics.
Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Kidney transplant recipients
Collection of data from kidney transplant patients at regular outpatient check-ups.
No intervention
No intervention
Interventions
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No intervention
No intervention
Eligibility Criteria
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Inclusion Criteria
* Recipient of a transplanted kidney
* Planned visit to the outpatient nephrology clinic of University Hospital Ostrava, Czech Republic, between 1.5. and 30.7.2021 for enrolment
* Planned blood collection and available results of blood tests from planned inspections from 18.1.2021.
* Signed consent to the use of anonymous data for scientific purposes and publications.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital Ostrava
OTHER
Responsible Party
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Principal Investigators
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Jan Vaclavik, prof.,M.D.
Role: STUDY_CHAIR
University Hospital Ostrava
Locations
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University Hospital Ostrava
Ostrava, , Czechia
Countries
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Other Identifiers
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2/IK-FNO/2021
Identifier Type: -
Identifier Source: org_study_id
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