The purpose of this study is to investigate the efficient vaccine type as a booster dose for Coronavirus Disease of 2019 (COVID-19) in solid organ transplant recipients.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Patients 18 years of age and older
* Patients who had received a solid organ (kidney, liver, lung, heart, and pancreas) transplant patient from living or deceased donors.
* Patients with active graft with at least one immunosuppressive medication
* Completed two doses of BNT162b2 vaccination at least 28 days ago
Exclusion Criteria:
* Patient with non-active graft
* Any significant side effect with previous COVID-19 vaccination
* Within 28 days of BNT162b2 vaccine completion
* Already received more than and equal to three doses of COVID-19 vaccination
* Previously received COVID-19 vaccine other than BNT162b2 vaccine
* Previously received monoclonal Antibody treatment that are specifically directed against the spike protein for Severe Acute Respiratory Syndrome (SARS) Coronavirus 2 (CoV)-2 such as Mab, Bamlanivimab, etesevimab, Casirivimab, imdevimab, Sotrovimab and/or any combination.
* Thrombocytopenia (if less than 50,000 per microliter 30 days prior vaccination)
* History of Capillary Leak Syndrome
* Adults unable to consent
* Individuals who are not yet adults (younger than 18 year old)
* Vulnerable patients (prisoners)
* Pregnant women
What they're measuring
1
Percentage of Participants Who Tested Positive for IgG Antibodies to the Anti-spike Protein of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
Timeframe: Up to 1 month (post booster vaccination)