CTRI/2021/04/033143招募中3 期
A Multicenter Prospective, Open Label, Randomized, Clinical Study To Evaluate The Safety And Efficacy Of Cardamom-based capsules and sachets In Mild to Moderate Covid-19 Adult Patients
Zum Heilen Diagnostic Therapeutics ZH DT0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Subjects aged 18-75 years of age and of either sex
- •2.Subjects who are willing to give consent to the study
- •3.COVID-19 positive clinical symptoms and (subsequently) confirmed by the current recommended confirmatory test (RT-PCR).
- •4.Mild to Moderate disease (NEWS score Less than/equal to 8)
- •5.Can take oral medicines
- •6.Subject willing to abide by and comply with the study protocol
排除标准
- •1.Age less than 18 years and more than 75 years
- •2.Pregnancy and lactation
- •3.Severe or complicated course of COVID-19 disease
- •4.Presence of acute hypoxic respiratory failure/ need for Intensive care unit (ICU) stay/ Patients who need mechanical ventilation.
- •5.Any uncontrolled systemic disease, infection
- •6.Those with serious Cardiovascular, Cerebrovascular, Respiratory, Liver or Renal disease or any other disorder.
- •7.Other conditions, which in the opinion of the investigators makes the patient unsuitable for enrolment or could interfere in adherence to of the study protocol
研究者
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