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临床试验/jRCTs041200072
jRCTs041200072已完成不适用

COVID-19 Prevention of worsening of symptoms in asymptomatic to mild patients by combined use of kakkonto and hochuekkito: Exploratory open-label randomized controlled trial (HKCOV)

未提供0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
100
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Prevention Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • SARS-CoV-2 is positive in nucleic acid detection or antigen test.
  • 20years old or over
  • Asymptomatic or mild symptoms.

排除标准

  • Administration of kampo medicine (Juzendaihoto,Ninjinyoueito, Hochuekkito, Seishoekkito, Rikkunshito, Shikunshito, Kihito, Kamikihito) within the last two weeks
  • Persons with a history of hypersensitivity to Hochuekkito or Kakkonto
  • Those who participated in other clinical intervention studies (studies) within 3 months before the start of study drug administration
  • A person who is judged by the principal investigator or the investigator to be inappropriate as a research subject.
  • Those who are pregnant, may be pregnant, or are breastfeeding

结局指标

主要结局

-

The ratio of worsening within 10days after test drug administration

次要结局

  • Blood test
  • Changes in Kampo findings
  • CT findings
  • Deterioration rate(28th day)
  • Examination of antibodies before and after administration(28 days later)
  • Comparison before and after(10-day observation period)

研究者

发起方
未提供

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