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临床试验/NCT03031743
NCT03031743已完成不适用

Nested Case-control Analysis of the Influence of the Microbiome on Rotavirus Vaccine Immunogenic Response in Infants in Karachi, Pakistan

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)1 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2014年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
88
试验地点
1
主要终点
differences in fecal microbiota composition

研究概览

简要总结

This is a nested case-control study within an ongoing rotavirus vaccine immunogenicity trial in Karachi, Pakistan. The primary study aim is to compare the fecal microbiota composition and diversity of infants who do (control) and do not (case) demonstrate immune seroconversion to rotavirus vaccination. The infants will be matched for vaccination dose, age and breast-feeding practices.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
6 Weeks 至 3 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Infants already consented and enrolled in the overarching study: Immunogenicity of Rotavirus Vaccine Under Different Age Schedules and the Impact of Withholding Breast Feeding around the Time of Vaccination on the Immunogenicity or Rotarix Vaccine trial (NCT01199874)
  • Overarching study (NCT01199874)inclusion criteria:
  • 6 weeks 0 days to 7 weeks 6 days age at the time of enrollment
  • Healthy infant free of chronic or serious medical condition as determined by history and physical exam at time of enrollment
  • written informed consent obtained from parents or guardians for overarching study Nested study additional inclusion criteria
  • written informed consent obtained from parents or legal guardians for this nested study
  • availability of a baseline, pre-vaccination fecal sample

排除标准

  • Overarching study (NCT01199874)exclusion criteria
  • hypersensitivity to any of the vaccine components
  • Use of any investigational drug or vaccine other than the study vaccine within 30 days of first dose of study vaccine or during the study
  • use of any immunosuppressive drugs
  • previous intussusceptions or abdominal surgery
  • enrollment in any other trials
  • birth weight less than 1500 grams; or if birthweight is unknown, weight less than 2000 grams on or before 28 days
  • immunoglobulin and/or blood products use since birth or during the study period Nested study additional exclusion criteria
  • positive serum anti-rotavirus IgA (> or= 20U/mL) at 6 weeks of age, indicative of rotavirus infection prior to vaccination

结局指标

主要结局

differences in fecal microbiota composition

时间窗: 2 years

The primary study objective is to see if there are significant differences in the fecal microbiota composition between rotavirus vaccine (Rotarix TM) immune responders (defined as anti-RV IgA antibodies at a concentration of \> or = to 20 U/ml in a previously seronegative individual 4 weeks after the last Rotarix dose) and rotavirus vaccine immune non-responders (defined as anti-RV IgA antibodies at a concentration of \<20 U/mL 4 weeks after the last Rotarix dose)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vanessa Harris

Principal Investigator

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (1)

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