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Prevalence and Outcome of SARS-CoV-2 Infection & COVID-19 in Transplant Recipients: The COVITRA Study

Prevalence and Outcome of SARS-CoV-2 Infection in Solid Organ and Hematopoietic Cell Transplant Recipients: The COVITRA Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04579471
Acronym
COVITRA
Enrollment
2000
Registered
2020-10-08
Start date
2020-07-01
Completion date
2025-12-31
Last updated
2024-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, SARS-CoV Infection, Transplantation Infection

Keywords

covid19, SARS-CoV Infection, transplantation

Brief summary

This project will provide novel data using a large cohort of more than 3000 transplanted patients. Risk and protective factors for SARS-CoV-2 infection and COVID-19 disease severity will be identified. The proportion of patients who develop antibodies after infection will be revealed. In this way the presence of these antibodies can be evaluated as a test for prior infection. Our study additionally will demonstrate how long these antibodies remain present and whether they are protective against a new infection.

Interventions

DIAGNOSTIC_TESTSARS-CoV-2 IgG

Collection of clinical variables, assessment of IgG antibodies for SARS-CoV-2, plasma collection for translational immunology studies

Sponsors

KU Leuven
CollaboratorOTHER
Hasselt University
CollaboratorOTHER
Ziekenhuis Oost-Limburg
CollaboratorOTHER
Jessa Hospital
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* all patients who underwent solid organ or hematopoietic cell transplantation at UZ Leuven and who give informed consent

Exclusion criteria

* age under 18 years

Design outcomes

Primary

MeasureTime frameDescription
Prevalence and risk-factors for SARS-CoV-2 infectioninclusion during 4 monthsPrevalence and risk-factors for SARS-CoV-2 infection
Prevalence and risk-factors for COVID-19inclusion during 4 monthsPrevalence and risk-factors for COVID-19

Secondary

MeasureTime frameDescription
Durability of IgG positivity12 monthsDurability of IgG positivity/immunity

Countries

Belgium

Contacts

Primary ContactJef Verbeek, MD, PhD
jef.verbeek@uzleuven.be+ 32 16 34 42 25
Backup ContactNatalie Van den Ende
natalie.vandenende@uzleuven.be+32 16 340749

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026