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临床试验/SLCTR/2018/024
SLCTR/2018/024尚未招募2 期

Efficacy and safety of oral hydroxyurea in transfusion dependent beta-thalassaemia: a randomized double-blind placebo-controlled clinical trial

Faculty of Medicine - University of Kelaniya0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Male and female patients with confirmed genotype of homozygous or compound heterozygous beta-thalassaemia major or HbE beta-thalassaemia
  • 2. Age above 12 years
  • 3. Patients who required more than 10 transfusions during the preceding year

排除标准

  • 1. Patients who have undergone bone marrow transplantation
  • 2. Patients with very high serum ferritin (>5000ng/ml)
  • 3. Sickle beta-thalassaemia
  • 4. Chronic liver disease
  • 5. Chronic kidney disease
  • 6. Patients with contraindications for hydroxyurea therapy (eg: hypersensitivity, severe anaemia with haemoglobin less than 5g/dl at the beginning of treatment, bone marrow depression, pregnancy and lactation)
  • 7. Patients who are expecting to get pregnant during next 12 months
  • 8. White blood cell count less than 4000/uL.
  • 9. Platelet count less than 150,000/uL.
  • 10. Evidence of active viral infection, including viral hepatitis
  • 11. Patients on immunosuppressant therapy

研究者

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