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临床试验/CTRI/2010/091/000299
CTRI/2010/091/000299招募中2 期

Rationalization of single dose 10 mg/kg/bw and 15 mg /kg/bw as compared to 5 mg/kg/bw for four days of Liposomal Amphotericin B with special reference to efficacy and safety profile for treatment of visceral leishmaniasis in Bihar, India

ICMR0 个研究点目标入组 180 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
180

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

  • Male and female of age between 08-60 years (inclusive)
  • Clinical signs and symptoms compatible with Kala-azar (e.g.. fever, splenomegaly, anaemia,
  • leucopenia)
  • Confirmed diagnosis of VL by visualization of parasites on splenic/bone marrow aspirate
  • Written informed consent from the patient/or from parent or guardian if under 18 years old

排除标准

  • Safety concerns:
  • Hemoglobin < 5 g/dl
  • White blood cell count < 1000/mm3
  • Platelets <50,000
  • Prothrombin time > 5 sec above control
  • ASAT > 3 times the upper limit of normal
  • Serum creatinine or BUN > 1.5 times the upper limit of normal
  • HIV positive serology
  • Tuberculosis

研究者

发起方
ICMR

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