The Use of Isatidis Root and Forsythia Oral Liquid for the Treatment of Mild Cases of COVID-19: A Trial Clinical Study
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
- 否
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
干预措施: Langenlianqiao (Drug)
LHQW group
干预措施: LianhuaQingWen (Drug)
placebo control group
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
Mi Zhou
Investigator
Central South University
