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临床试验/TCTR20230929001
TCTR20230929001
尚未招募
4 期

Reduced Dose Pneumococcal Conjugate Vaccine Schedules: Closing the Knowledge Gap and Informing Immunization Policies in Thailand

The National Vaccine Institute (NVI), Thailand0 个研究点目标入组 1,050 人2023年9月29日

概览

阶段
4 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
The National Vaccine Institute (NVI), Thailand
入组人数
1050
状态
尚未招募
最后更新
去年

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2023年9月29日
结束日期
2025年12月1日
最后更新
去年
研究类型
Interventional
性别
All

研究者

发起方
The National Vaccine Institute (NVI), Thailand

入排标准

入选标准

  • 1\)Female or male infants aged 2 months (plus/minus 7 days).
  • 2\)Participants with normal birthweight.
  • 3\)Participants born to HIV\-uninfected mothers.
  • 4\)Participants that have parent or legal caregiver capable of comprehending Thai (speaking, reading, writing) and abiding by protocol instructions.
  • 5\)Participants that have parent or legal caregiver that are available throughout the trial period.
  • 6\)Participants that have parent or legal caregiver willing to provide written inform consent to have their children participate in the clinical trial.

排除标准

  • 1\)Participants with severe illnesses, unmanageable symptoms, or underlying unstable disease.
  • 2\)Participants with a history of pneumococcal disease (microbiologically confirmed).
  • 3\)Participants with a history of severe drug or vaccine allergies (anaphylaxis), especially PCV or vaccines that contain diphtheria toxoid.
  • 4\)Participants with Streptococcus pneumoniae vaccination history.
  • 5\)Participants that received any vaccines within 14 days of screening and enrollment.
  • 6\)Participants that received plasma, immunoglobulins, antivirals, antibodies, or blood transfusions, products, or components within 90 days prior to screening and enrollment.
  • 7\)Participants with a fever (greater than 37\.2 degree celsius under the arm) at screening or baseline.
  • 8\)Participants with a history of immunodeficiencies or immunocompromise since, or soon after, birth.
  • 9\)Participants with severe cardiovascular, digestive, pulmonary, endocrine, or central nerve system illness since, or soon after, birth.
  • 10\)Participants with other clinically significant reason, as determined by the investigator, that may affect immune responses to PCV.

结局指标

主要结局

未指定

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