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临床试验/TCTR20211023002
TCTR20211023002已完成4 期

Safety, tolerability, and antibody response after intradermal vaccination of COVID-19 vaccine; PFE-BNT in adults who have completed two-doses of Verocell (inactivated vaccine)

ampang Hospital0 个研究点目标入组 42 人开始时间: 2021年10月23日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
42

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • participants were adults aged more than 18 years who completed 2 doses of a three-week schedule of Verocell, and have not had SARS-CoV-2 infection.

排除标准

  • Participants were excluded from the study if they: had history of severe adverse or allergic reactions to previous vaccinations, were pregnancy or planned pregnancy within 4 weeks after vaccination, used of systemic or topical corticosteroids, had bleeding diathesis , received other Covid-19 vaccine, and had SARS-CoV-2 infection before collecting post ID injection blood sample.

研究者

发起方
ampang Hospital

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