跳至主要内容
临床试验/EUCTR2011-002667-14-CZ
EUCTR2011-002667-14-CZ进行中(未招募)1 期

Effect of vaccination in patients with recurrent respiratory papillomatosis– can we improve the quality of life of these patients?

Institute of Hematology and Blood Transfusion0 个研究点目标入组 50 人开始时间: 2011年6月30日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

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

入选标准

  • Patients with RRP which sign the informed consent form with both parts of the study will be enrolled.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • Patients who experience severe side effects of vaccination after the first or second dose will not be vaccinated with the third dose and they will be excluded from the study. Patients who will not receive all three doses within one year and 30 days will be also excluded.

研究者

发起方
Institute of Hematology and Blood Transfusion

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