跳至主要内容
临床试验/EUCTR2004-005028-42-GB
EUCTR2004-005028-42-GB进行中(未招募)不适用

A prospective, multi-centre, phase III-b study of TachoSil in paediatric patients scheduled for resection of the liver with or without segmental liver transplantation - TachoSil paediatric liver study

ycomed Danmark ApS0 个研究点目标入组 40 人开始时间: 2006年1月13日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Infomed consent obtained from the parents(s)/legal gurdian.
  • Minor or moderate haemorrhage from the cut surface after liver resection with or without segmental liver transplantation and after primary haemostatic treatment. Age above 4 weeks and below 6 years.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Congenital coagulation disorders. Serious surgical complications. Hypersensitivity to the active substances or to any of the excipients.

研究者

发起方
ycomed Danmark ApS

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