A Study to Evaluate the Safety and Efficacy of KOVIR in the Combination Regimen With Background Treatment in COVID-19 Patients Without Symptoms of Acute Respiratory Distress
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 66
- 试验地点
- 2
- 主要终点
- Change in the severity of daily symptoms
研究概览
简要总结
The acute pneumonia pandemic caused by a new strain of corona virus 2019 named as COVID-19 by the World Health Organization (WHO) is a pandemic caused by SARS-CoV-2 virus. The reported symptoms vary from fever or chills, cough, shortness of breath, to muscle aches, headaches, loss of taste or smell.
The hard capsule KOVIR is a product based on the traditional medicine named "Nhân sâm bài độc táng" which is used to treat the cold conditions, also known as the initial plague according to the theory of traditional medicine.
详细描述
The acute pneumonia pandemic caused by a new strain of corona virus 2019 named as COVID-19 by the World Health Organization (WHO) is a pandemic caused by SARS-CoV-2 virus. The reported symptoms have included, but are not limited to fever or chills, cough, shortness of breath, muscle aches, headaches, loss of taste or smell, diarrhea, dizziness, sore throat, abdominal pain, anorexia, and vomiting.
The hard capsule KOVIR is a product based on the traditional prescription named "Nhân sâm bài độc táng" which is used to treat the cold conditions, also known as the initial plague according to the theory of traditional medicine.
The study timeline is expected about 7 months, including enrolment period, 14 days of treatment, data entry and analysis.
The study compares between standard dose regimen of KOVIR combined with background treatment in COVID-19 patients and placebo combined with background treatment in COVID-19 patients.
All participants will be treated and followed up in 14-day period. In case the participant meets the discharge criteria before 14 days, discontinuing the study drug will be done at the discretion of the investigators.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female, age from 18 to 65 years old, Vietnamese nationality
- •Participants diagnosed with Positive result of SARS-CoV-2 using real time RT-PCR test, Ct value <30 (equivalent to viral load > 3log)
- •Voluntary participation in the study by signing an informed consent
- •Ability to adhere to treatment according to the investigator's assessment
排除标准
- •Symptoms of severe upper and lower respiratory tract infections such as dyspnea, SpO2<93%.
- •Acute reduction of ventilation function of respiratory apparatus and/or respiration function of the lung in any of the following three groups:
- •Respiratory distress due to hypoxemia with PaO2 less than 60mmHg when breathing room air.
- •Respiratory distress due to hypercapnia with PaCO2 above 50mmHg
- •Mixed respiratory distress accompanied by both a decrease in PaO2 and an increase in PaCO2
- •Allergy/intolerance to any component of the study drug.
- •Inability to administer medicine.
- •Severe pneumonia as assessed by the investigator.
- •Inability to comply with study procedures or to ensure compliance with study drug administration as assessed by investigators.
结局指标
主要结局
Change in the severity of daily symptoms
时间窗: up to 14 days
Scale: 0 = Asymptomatic, 1 = Mild, 2 = Moderate, 3 = Severe
Change in viral load of SARS-CoV-2
时间窗: up to 14 days
Daily assessment using qRT-PCR test
The time from baseline to the peak of viral load of SARS-CoV-2
时间窗: up to 14 days
Daily assessment using qRT-PCR test
The time from baseline to no SARS-CoV-2 virus detection
时间窗: up to 14 days
Daily assessment using qRT-PCR test
Number of participants without SARS-CoV-2 virus detection after 7 days of treatment
时间窗: after 7 days of treatment
Assessment using qRT-PCR test
Number of participants without SARS-CoV-2 virus detection after 14 days of treatment
时间窗: after 14 days of treatment
Assessment using qRT-PCR test
The cell counts of TD4 and TD8 change from 7 days to 14 days of treatment
时间窗: at day 7 and 14 days of treatment
Laboratory test of TD4 and TD8
Number of participants with respiratory distress complications requiring treatment
时间窗: up to 14 days
Appearance of symptoms of respiratory distress complications requiring treatment
Number of Participants with Adverse Events as Assessed by CTCAE v5.0
时间窗: up to 30 days after last dose
Study drug-related adverse events, adverse events leading to study termination, serious adverse events (SAE)
次要结局
未报告次要终点