跳至主要内容
临床试验/ISRCTN38082350
ISRCTN38082350已完成不适用

Dose-response study of 17DD yellow fever vaccine produced by Bio-Manguinhos/Fiocruz

Bio-Manguinhos/Fiocruz (Brazil)0 个研究点目标入组 1,050 人开始时间: 2008年12月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,050

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

性别
Male

入选标准

  • 1. Adult men
  • 2. Aged 18 - 30 years old
  • 3. Healthy
  • 4. Agree to participate after reading and understanding Free and Informed Consent Form

排除标准

  • 1. Prior vaccination against yellow fever
  • 3. Use of immunosuppressor drugs in the last 12 months
  • 4. Personal history of autoimmune diseases
  • 5. Personal history of thymus diseases
  • 6. Personal history of anaphylactic reactions to foods, drugs or vaccines
  • 7. Personal history of allergy to eggs, erythromycin, canamycin or gelatin
  • 8. Persons who received immunoglobulin, blood transfusions or blood derivatives in the last 12 months
  • 9. Persons who received live virus vaccines or cholera vaccine in the last 30 days or who plan to receive them in the following 30 days after yellow fever vaccination

研究者

发起方
Bio-Manguinhos/Fiocruz (Brazil)

相似试验