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临床试验/EUCTR2011-004457-87-Outside-EU/EEA
EUCTR2011-004457-87-Outside-EU/EEA进行中(未招募)不适用

A Phase III, randomized, blind-observer, controlled, multicenter trial in 412 infants in Thailand.

Sanofi Pasteur S.A0 个研究点目标入组 412 人开始时间: 2012年4月10日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
412

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

  • 1) Two-month-old infant (50 to 71 days old) on the day of inclusion, of either gender
  • 2) Born at full term of pregnancy (=37 weeks) and with a birth weight =2.5 kg
  • 3) Hepatitis B vaccination since birth
  • 4) Informed consent form signed by one parent/legally acceptable representative and an independent witness if the parent/legally acceptable representative is illiterate
  • 5) Able to attend all scheduled visits and to comply with all trial procedures
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 412
  • 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

  • 1) Participation in another clinical trial in the 4 weeks preceding the first trial vaccination
  • 2) Planned participation in another clinical trial during the present trial period
  • 3) Systemic hypersensitivity to any of the vaccine components or history of a life-threatening reaction to the trial vaccine or a vaccine containing the same substances
  • 4) Congenital or acquired immunodeficiency, or immunosuppressive therapy such as long-term systemic corticosteroid therapy
  • 5) Chronic illness at a stage that could interfere with trial conduct or completion
  • 6) Blood or blood-derived products received since birth
  • 7) Any vaccination in the 4 weeks preceding the first trial vaccination
  • 8) Any planned vaccination (except trial vaccinations) during the trial
  • 9) Documented history of pertussis, T, D, polio, Hib, hepatitis B or Streptococcus pneumoniae infection(s) confirmed either clinically, serologically, or microbiologically
  • 10) Previous vaccination against pertussis, T, D, poliomyelitis, Hib infection(s) or Streptococcus pneumoniae
  • 11) Known personal or maternal history of Human Immunodeficiency Virus (HIV), Hep B (HBsAg carrier), or Hepatitis C seropositivity
  • 12) Known thrombocytopenia or bleeding disorder contraindicating IM vaccination
  • 13) History of seizures
  • 14) Febrile (rectal equivalent temperature =38.0°C) or acute illness on the day of inclusion

研究者

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