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临床试验/TCTR20220301002
TCTR20220301002已完成不适用

ong term immunogenicity of BNT162b2 vaccination and attitudes toward COVID-19 booster vaccines in Thai children

Ratchadapisek Research Funds0 个研究点目标入组 240 人开始时间: 2022年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
240

研究概览

简要总结

A booster dose of BNT162b2 elicits high immunogenicity against the Omicron variant. Motivation for receiving booster doses is to reduce risk of infection

研究设计

研究类型
Observational

入排标准

年龄范围
5 Years 至 18 Years(—)
性别
All

入选标准

  • 1. Participants must age 5 to <18 years old on the day of first dose vaccination, 2. Participants must be completed second dose of BNT162b2 vaccine for 6 months at the time of data collection, 3.Participants must be in good health at the time of entry into the trial as determined by medical history, physical examination (including vital signs), and the clinical judgment of the investigator, 4.Participants and parent(s) must be able to communicate effectively with study personnel and considered reliable, willing, and cooperative in terms of compliance with the protocol requirements, 5.Participants and/or parent(s) or legally authorized representative(s) must sign a written informed consent form, including any required privacy authorization form, prior to the initiation of any trial procedures, after the nature of the trial has been explained according to local regulatory requirements

排除标准

  • 1. Participants with previous documented SARS-CoV-2 infection, 2. Receipt of immunoglobulins or blood products between the day of first vaccination and blood collection, 3.Receipt of any other vaccines within 14 days (for inactivated vaccines except influenza vaccine) or 28 days (for lived vaccines) prior to blood collection, 4. Use of any medications that may be associated with impaired immune responsiveness or with immunosuppression.

研究者

发起方
Ratchadapisek Research Funds

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