CTRI/2012/05/002675已完成未知
PROSPECTIVE OBSERVATIONAL STUDY OF ROTAVIRUS INFECTION IN INFANTS IN SEWAGRAM, MAHARASHTRA, INDIA TO PREPARE FOR A PROPOSED ROTAVIRUS VACCINE EFFICACY TRIA
Serum Institute of India Ltd Pune0 个研究点目标入组 800 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 800
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •For all participants:
- •1.Healthy infants as established by medical history and clinical examination before entering into the study.
- •2.Parental / legal guardian ability and willingness to provide informed consent.
- •3.Parent / legal guardian who will remain in the area during the study period.
- •Additional criteria for cohort 1:
- •4.Age: 6-8 weeks at the time of enrollment.
- •Additional criteria for cohort 2:
- •5.Age: 8-12 months at the time of enrollment.
排除标准
- •1.Presence of diarrhea or vomiting in the previous 24 hours or on the day of enrolment (temporary exclusion).
- •2.Presence of high fever on the day of enrolment (temporary exclusion).
- •3.History of congenital abdominal disorders, intussusception, abdominal surgery or any other congenital disorder.
- •4.Known or suspected impairment of immunological function based on medical history and physical examination.
- •5.Subjects who have received rotavirus vaccine.
- •6.History of chronic diarrhea (defined as diarrhea more than 14 days).
- •7.Subject parents who will not be available or willing for active weekly follow-up by the study staff.
- •8.Chronic administration (defined as more than 14 days) of immunosuppressants including corticosteroids since birth. Infants on inhaled or topical steroids may be permitted to participate in the study.
- •9.History of any neurologic disorders or seizures.
- •10.Any medical condition in the parents / legal guardian / infants that, in the judgment of the investigator, would interfere with or serves as a contraindication to protocol adherence or a participantâ??s ability to give informed consent.
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