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临床试验/NCT01906190
NCT01906190已完成不适用

Persistence Study of Immune Response After Vaccination With Influenza Vaccine in Healthy Population

Centers for Disease Control and Prevention, China1 个研究点 分布在 1 个国家目标入组 207 人开始时间: 2011年8月1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
207
试验地点
1
主要终点
change from serum antibodies against vaccine-related influenza virus at 6,12,18,24 months

研究概览

简要总结

This clinical study will be performed in subjects aged 12-60 years old enrolled in NCT01310374 who received 2010 seasonal influenza vaccine to evaluate the persistence of the immune response of influenza vaccine up to 24 months after vaccination.

详细描述

Subjects were previously vaccinated at 12 to 60 years of age with 2010 seasonal influenza vaccine.The persistence phase starts 24 months after the primary vaccination and blood samples will be taken at 6, 12, 18 and 24 months after primary vaccination. Subjects whose antibody titer less than 1:40 at 6 months after primary vaccination will receive a booster dose of influenza vaccine.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
12 Years 至 60 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • aged 12-60 years old
  • male or non-pregnant female
  • volunteers received 2010 seasonal influenza vaccine
  • clinically healthy as determined by: medical history inquiring and physical examination
  • provide written informed consents before joining the trial

排除标准

  • without history of 2010 seasonal influenza vaccine administration,
  • allergic to any ingredient of vaccine,
  • autoimmune disease or immunodeficiency,
  • severe adverse reaction after vaccination, such as allergies, hives, breathing difficulties, angioedema or abdominal pain,
  • severe acute and chronic diseases
  • axillary temperature over 37.0℃ at the time of vaccination.

结局指标

主要结局

change from serum antibodies against vaccine-related influenza virus at 6,12,18,24 months

时间窗: 6,12,18,24 months after the primary vaccination

Persistence of antibodies in all subjects with respect to components of the investigational vaccine - month 6,12,18,24

次要结局

未报告次要终点

研究者

发起方
Centers for Disease Control and Prevention, China
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Wu Jiang

Department of Immunization & Prevention, Beijing Centers for Disease Control and Prevention

Centers for Disease Control and Prevention, China

研究点 (1)

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