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临床试验/IRCT2015061822805N1
IRCT2015061822805N1已完成1 期

The efficiency of recombinant human erythropoietin in reducing the need for blood transfusions in patients with solid tumors receiving chemotherapy.

Vice Chancellor for research of Tabriz University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
60

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

年龄范围
1 year 至 15 years(—)
性别
All

入选标准

  • Age of the patients, entering the study, should be beneath 15 years; The amount of Hemoglobin should be below 10 g/dL(gram per deciliter); Patients who are anemic due to chemotherapy, after they are diagnosed with solid insitu tumor; None of the patients have bone marrow involvement; Patients entering the study have normal kidney,liver,and lung function; Normal amounts of other blood-related parameters including retic.count, Serum ferritin, B12 vitamin in the serum, direct and indirect coombs tests, and ABG(Arterial Blood Gas); No history of blood transfusions in the last 1 month; No history of Erythropoietin consumption
  • Exclusion criteria: Severe bleeding during the study; Hemolysis during the study due to any causes; The evidence of existing imapirment in kidney,liver,and lung function; Evidence of any serious side effects of Erythropoietin including thrombosis, increased systemic blood pressure, and polycythemia

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Tabriz University of Medical Sciences

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