跳至主要内容
临床试验/IRCT2015012620818N1
IRCT2015012620818N1已完成未知

Comparison the efficacy of Deferoxir versus other desferoxamine products in thalassemia major patient

exir pharmacutical company0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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
5 years 至 no limit(—)
性别
All

入选标准

  • Patients with major thalassemia under regular blood injection therapy;. age over 5; undergoing treatment with one of deferoxamine pharmaceutical products; Norma renal function; serum cratinine undr 0. 7; in children under the age of 12 less than 1.0; in teenagers less than 1.1; and in over 16 years old pateinets (female less than 1.2; male less than 1.2); Trans aminase enzymes level less than 2 times of normal range; BUN<22mg/dl.

排除标准

  • Any experience of allergic reaction to desferoxamine, positive HCV Ab / HBS Ag.

研究者

发起方
exir pharmacutical company

相似试验