A Study of Shengxuening Tablet in the Treatment of Chemotherapy-related Anemia in Hematologic Tumors
Hematological Malignancy, Cancer-Related Anemia
About this trial
This is an interventional treatment trial for Hematological Malignancy focused on measuring Shengxuening tablet, chemotherapy-related Anemia
Eligibility Criteria
Inclusion Criteria: Age>18 years old, gender is not limited; Patients diagnosed with blood cancer complicated with anemia; During the screening period of ≤1 week, hemoglobin (Hb): 60g/L<Hb≤100g/L; Willingness to treat Exclusion Criteria: During the screening period of ≤1 week, hemoglobin (Hb)≤60g/L History of blood transfusion within 1 month; Urgent blood transfusion or EPO infusion is required within the screening period of ≤1 week; Folic acid or vitamin B12 deficiency; History of iron allergy, history of allergy or intolerance to the study drug; Pregnant and lactating women; Age <18 years old and body weight ≤35kg; Participated in other clinical drug research in the past 3 months; Severe cardiac insufficiency (NYHA grade III or above); Severe abnormal liver function (ALT, AST and TBIL ≥ 2 times the upper limit of normal value); Severe renal insufficiency (creatinine clearance ≤ 15ml/min); Severe mental disorder; Acute and chronic blood loss; Combined with a second tumor; Ferritin>500μg/L; Combined with active tuberculosis; Failure to cooperate with treatment according to doctor's advice.
Sites / Locations
- Zhongnan Hospital of Wuhan UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Shengxuening Tablets
ferrous succinate
Oral treatment with Shengxuening Tablets 1 week before chemotherapy, usage: 0.5gtid, for 28 consecutive days
Oral treatment with ferrous succinate 1 week before chemotherapy, usage: 200mgqd, for 28 consecutive days