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临床试验/NCT06355193
NCT06355193已完成1 期

The Use of Isatidis Root and Forsythia Oral Liquid for the Treatment of Mild Cases of COVID-19: A Trial Clinical Study

Central South University1 个研究点 分布在 1 个国家目标入组 253 人开始时间: 2022年11月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
253
试验地点
1
主要终点
Treatment and symptomatic improvement effects of LGLQ

研究概览

简要总结

This study has significant implications for research, as it provides a basis for further studies on the antiviral effects of LGLQ Oral Liquid, encouraging more extensive clinical studies in larger populations and diverse age groups to validate these findings. For medical practice, the findings suggest that LGLQ can be considered an alternative treatment option for mild cases of COVID-19, especially in managing symptoms like fatigue, potentially broadening the range of effective treatments available to healthcare practitioners. In terms of policy, the demonstrated efficacy of LGLQ could lead to its inclusion in treatment guidelines for COVID-19 and other viral infections, fostering a more integrated approach combining Western medicine and Traditional Chinese Medicine in the global fight against pandemics. The insights from this study might prompt health policymakers to reassess the potential of herbal formulations in managing and treating infectious diseases and consider them in the development of future healthcare strategies and policies.

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

  • the diagnosis of SARS-Cov-2 infection confirmed by quantitative polymerase chain reaction (qPCR) test
  • aged 18 years or older
  • patients received more than 2 doses of SARS-Cov-2 vaccine
  • asymptomatic or mild at the time of hospitalization

排除标准

  • patients with malignant diseases, autoimmune diseases, liver and kidney diseases, blood diseases, neurological diseases, endocrine diseases and other serious diseases may affect the patient's participation in the trial or affect the results of the study
  • pregnant women, lactating mothers; allergic conditions
  • allergic to the known components of the drug
  • patients vaccinated with vaccines less than 1 shot
  • Patient does not agree to participate in this study

研究组 & 干预措施

LGLQ group

Experimental

干预措施: Langenlianqiao (Drug)

LHQW group

Experimental

干预措施: LianhuaQingWen (Drug)

placebo control group

Placebo Comparator

干预措施: placebo control group (Other)

结局指标

主要结局

Treatment and symptomatic improvement effects of LGLQ

时间窗: 1 month

LGLQ and LHQW were able to significantly reduce the duration of infection with novel coronaviruses

次要结局

未报告次要终点

研究者

发起方
Central South University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mi Zhou

Investigator

Central South University

研究点 (1)

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