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临床试验/NCT04480398
NCT04480398已完成不适用

A Retrospective Study on Efficacy and Safety of Guduchi Ghan Vati for Covid-19 Asymptomatic Patients

Aarogyam UK1 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2020年5月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
91
试验地点
1
主要终点
Virologic clearance

研究概览

简要总结

Coronavirus disease 2019 (Covid-19) has been declared global emergency with immediate safety, preventative and curative measures to control the spread of virus. Confirmed cases are treated with clinical management as they are diagnosed but so far, there is no effective treatment or vaccine yet for Covid-19.

With recommended guidelines of AYUSH Ministry, India, the use of Ayurveda for Covid-19 has increased; however, its efficacy and safety in Covid-19 confirmed patients remain unclear.

Present study examined the efficacy and safety of one of the recommended Ayurveda drug (Guduchi Ghan Vati) compared with standard care for patients with asymptomatic Covid-19 patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age over 18
  • A person diagnosed with COVID-19
  • Asymptomatic at the time of admission

排除标准

  • Patients over 75 years
  • Taking antibiotics or antiretroviral for any reason
  • Mild to Moderate symptoms at the time of hospital admission

研究组 & 干预措施

Ayurveda

Guduchi Ghan Vati was given to Covid patients 2 tablets (500 mg each) twice daily were given orally after meal for 28 days. Guduchi ghan vati is a powdered aqueous extract of Tinospora cordifolia in tablet form and prepared in GMP certified Pharmacy of the University, following standard protocol.

干预措施: Guduchi Ghan Vati (Drug)

结局指标

主要结局

Virologic clearance

时间窗: 21 days

Virologic clearance indicates the duration from the first Covid-19 positive result to the first Covid-19 negative result

次要结局

  • Change in the number of patients going from asymptomatic to moderately disease(10-days of hospital admission)
  • Hospital Stay(21 days)
  • Clinically relevant adverse effects(21-days)

研究者

发起方
Aarogyam UK
申办方类型
Other
责任方
Sponsor

研究点 (1)

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