跳至主要内容
临床试验/CTRI/2020/06/026197
CTRI/2020/06/026197尚未招募Phase 3 4

To Evaluate the Efficacy of SUDARSHAN GHAN VATI and VYAGHRADI KWATH in the management of patients with COVID-19- A Pilot study.

Ministry of AYUSH GoI1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年6月7日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Decrease in duration of conversion from COVID positive to negative

研究概览

简要总结

The world is witnessing Global Pandemic COVID -19. The lack of approved effective drug therapeutic protocol for COVID-19 would be a challenge for the treatment of the newly merged COVID -19 infections world wide. Ayurveda medicine is already being used in many states to prevent and cure the disease. Aim of this proposal is to evaluate the efficacy of Sudarshan Ghan Vati and Vyaghradi Kwath in the management of mild to moderate symptoms of COVID-19 positive patients. The trial will be conducted at Government Ayurvedic Hospital, Department of ISM&H, Government of J&K, Indira Chowk, Jammu, Government Medical College, Bakshi Nagar, Jammu and 200 bedded (Maternity) designated COVID hospital, Gandhi Nagar, GMC, Jammu. This study will be collaborative with duration of three months. The subjects will be randomly divided in two groups: Conventional treatment group and Ayurvedic & Conventional group. Sample size would be 60 and intervention time will be one month. Ethical clearance and consent is already taken. Laboratory investigations , assessment and follow up will be done as per methodology. Financial burden can be reduced if the result is found positive.

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Open Label

入排标准

年龄范围
1.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients of COVID-19 positive cases with mild to moderate symptoms
  • Patients who can take medicine orally
  • Patients willing to provide signed informed consent.

排除标准

  • Patients with severe symptom
  • Immuno compromised patients
  • Pregnant / Lactating females
  • COVID-19 negative patients.

结局指标

主要结局

Decrease in duration of conversion from COVID positive to negative

时间窗: 4 Weeks

次要结局

  • Improvement in Quality of Life(30 days)

研究者

发起方
Ministry of AYUSH GoI
申办方类型
Government funding agency

研究点 (1)

Loading locations...

相似试验