The study is to evaluate the safety and efficacy of COVID-19 convalescent plasma (CCP) transfusion to prevent COVID-19 in adult recipients following hematopoietic stem cell transplantation. 72 patients will be randomized in a 1:1 ratio to receive either CCR (36 patients) or not (36 patients). Patients in the CCP group will receive 200 ml of CCP at +14 days, +28 days, +2 months, and +3 months following hematopoietic stem cell transplantation. Patients in the control group would be routinely given oral ursodeoxycholic acid for +14 days after transplantation. The primary goal of the study is to evaluate the safety of CCP and the incidence of COVID-19 infection within +28 days after the last infusion of CCP.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
72
200 ml of COVID Convalescent Plasma at +14 days, +28 days, +2 months, and +3 months following hematopoietic stem cells transplantation.
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
Tianjin, None Selected, China
RECRUITINGTo evaluate the prevalence of new COVID infection
within +28 days after the last infusion of CCP
Time frame: 1 year
To evaluate the incidence of severe COVID-19
within +28 days after the last infusion of CCP
Time frame: 1 year
To evaluate the survival rate of COVID-19 infection
within 30 days after COVID-19 infection within +28 days after last CCP infusion
Time frame: 1 year
To evaluate the overall survival
at 1 year after transplantation.
Time frame: 1 year
To evaluate the tolerance of CCP infusion
at 1 year after transplantation.
Time frame: 1 year
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