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。
研究者
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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