42
Participants
Start Date
January 1, 2024
Primary Completion Date
December 31, 2024
Study Completion Date
February 1, 2025
complete blood count, CD3+ , CD4+ , CD8+, CD16+, CD56+, IFN-γ.
"1. Full history~2. Thorough clinical examinations~3. Laboratory investigations will include:~ 1. complete blood count with focus on platelet count, platelet distribution width and mean platelet volume. Platelet count will be confirmed by direct blood film and blood smear.~ 2. Measurements of CD3+, CD4+, CD8+ and natural killer cells (CD16+, CD56+) will be conducted using flow cytometry.~ 3. Serum IFN-γ levels will be determined using an ELISA kit.~4. Response to the treatment will be assessed according to The International Working Group criteria which defines Response as platelet count ≥ 30 x 10⁹/L and \>2-fold increase in platelet count from baseline and absence of bleeding, measured on 2 occasions greater than 7 days apart. No response is characterized by a platelet count \<30 x 10⁹/L or a less than 2-fold increase in platelet count from baseline, or the presence of bleeding."
Assiut University
OTHER