The Use of N-acetylcysteine for Thrombotic Events After Allogenic Hematopoietic Stem Cell Transplantation
Thrombotic Disorder
About this trial
This is an interventional prevention trial for Thrombotic Disorder focused on measuring Thrombotic disorder, Hematopoietic stem cell transplantation
Eligibility Criteria
Inclusion Criteria: Aged 16-70 years old Diagnosed as myeloid malignancies, and about to undergo allo-HSCT; ECOG: 0-2; Expected survival longer than 1 month Exclusion Criteria: Allergic to any components of NAC; Severe dysfunction of heart, liver, lung and kidney; Relapse before HSCT; A history of bronchial asthma, bronchospasm or moderate / severe gastrohelcosis.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Arm A
Arm B
Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion; N-acetyl-cysteine (Zambon Pharma, Hainan, China) : 8g/d (>=45kg); 200mg/kg.d (<45kg), intravenously for at least 4 hours, day -9 to day +45.
Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion.