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临床试验/NCT05017493
NCT05017493已完成1 期

Treatment of Early-Stage Covid-19 With a Herbal Compound, Xagrotin

Biomad AS1 个研究点 分布在 1 个国家目标入组 661 人开始时间: 2020年7月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
Biomad AS
入组人数
661
试验地点
1
主要终点
Mortality

研究概览

简要总结

This is an interventional, multi-center, randomized study. Adults with confirmed covid-19 disease not more than 10 days before enrollment date were recruited (n=361). Patients in same condition who had treated with standard of care were randomly assigned to the control group (n=178). The investigators analyzed the effect of a herbal compound, Xagrotin, and also investigated impact of different characteristics for instance gender, age, duration of disease, smoking habits and concomitant diseases on the outcome.

详细描述

This is an interventional, multi-center, randomized study that has been performed in an outpatient setting (n=361). Adults with confirmed covid-19 disease not more than 10 days before enrollment date were recruited. Patients in same condition who had treated with standard of care were randomly assigned to the control group (n=178). The investigators analyzed the effect of a herbal compound, Xagrotin, and also investigated impact of different characteristics for instance gender, age, duration of disease, smoking habits and concomitant diseases on the outcome. Adverse events were registered.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or higher
  • Newly diagnosed (no longer than 10 days)
  • PCR or clinically confirmed Covid-19

排除标准

  • Severe pulmonary disease
  • Severe cardiovascular disease
  • Severe hepatic disease
  • Severe renal disease
  • Diabetes mellitus type one
  • Metabolic acidosis
  • Oxygen saturation <70%
  • Pregnancy
  • Breast feeding
  • Concomitant treatment with anticoagulation drugs
  • Concomitant treatment with CYP3A4 medicines with narrow therapeutic window

结局指标

主要结局

Mortality

时间窗: 30 days

Number of Participants who died by day 30 after the enrollment

次要结局

  • Duration of Disease From Beginning of Treatment(30 days)
  • Duration of Hospitalization When Occurred(30 days)
  • Hospitalization(30 days)

研究者

发起方
Biomad AS
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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