Liver Transplant Clinical Trial
Official title:
Evaluation of the Immune Response to COVID-19 Vaccine in Recipients of Living Donor Liver Transplantation
A prospective cohort study to evaluate the response to COVID-19 vaccine in liver transplantation patients.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | November 30, 2023 |
Est. primary completion date | June 30, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age>18 - At least 3 month post transplantation Exclusion Criteria: - pediatric recipients - Active covid infection at the time of the study - Pregnancy - Allergy to any ingredients included in the vaccine - Lactation in first six month of delivery - Active Acute cellular rejection proven by liver biopsy - Acute Febrile state with either leucopenia or leucocytosis - High dose of corticosteroid at study timing (pulse methyl prednisolone) |
Country | Name | City | State |
---|---|---|---|
Egypt | Ain Shams center for organ transplantation (ASCOT), Ain shams university specialized hospital | Cairo | Please Select Region, State Or Province |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neutralizing antibody titer change 14 days after vaccination compared to baseline | neutralizing antibody response to SARS-CoV-2 vaccine in recipients post living donor liver transplantation | At baseline, at 14 days after whole course of vaccination | |
Primary | Neutralizing antibody titer change 28 days post vaccination compared to baseline | neutralizing antibody response to SARS-CoV-2 vaccine in recipients post living donor liver transplantation | At baseline and 28 days after whole course of vaccination | |
Secondary | Interleukin-6 serum level | Assessing the cellular immunological response to SARS-CoV-2 vaccine in recipients post living donor liver transplantation | At baseline, at 14 and 28 days after whole course of vaccination | |
Secondary | Incidence of confirmed coronavirus disease | Patient follow-up for confirmed symptomatic infection by SARS-COV2 virus | 28 days after whole course of vaccination | |
Secondary | Incidence of adverse events related to vaccine | Self reported safety and tolerability of vaccine | 7 days after each dose of the vaccine and up to 28 days after last vaccine dose administered | |
Secondary | Incidence of acute graft rejection | Follow-up for signs and symptoms of graft rejection | On 14 and 28 days post whole course vaccination | |
Secondary | Immune response correlation to HLA DRB1 genetic polymorphism | TaqMan®? SNP genotyping assay of HLA DRB1 gene (rs2647087) | 28 days post whole course vaccination | |
Secondary | Immune response correlation to IL-18 genetic polymorphism | TaqMan®? SNP genotyping assay of IL-18 gene (rs187238 and rs917997) | 28 days post whole course vaccination |
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