Ayurveda intervention as clinical trial against COVID-19

Phase 3

Not yet recruiting

• Conditions: COVID 19 virus identified. Ayurveda Condition: SANNIPATA-JVAROPADRAVAH,

• Registration Number: CTRI/2022/02/040562
• Lead Sponsor: All India Institute Of Ayurveda

Brief Summary

In the wake of COVID 19, an infectious disease caused by a newly discovered coronavirus,

entire mankind across the globe is suffering. Till date, no medicine or therapy has demonstrated

promising results in either preventing the disease or improving its prognosis to prevent this

infection.The intervention proposed under the project is a herbal combination based on traditional

knowledge of Ayurveda. The intervention is expected to improve quality of life of COVID

patients treated in addition to disease cure without major side effects.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-01-03
• Last Update Posted: 2022-02-21

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• 1.Newly diagnosed COVID-19 confirmed by RT-PCR.
• 2.Mild to Moderate COVID-19 infection.
• 3.Comorbid conditions (HTN, Diabetes, Metabolic Syndrome) 4.Willingness and ability to comply with trial and follow-up procedures.
• 5.Ability to understand the nature of this trial and give written informed consent.

Exclusion Criteria

• 1.Patients with severe and critical infection will be excluded.
• 2.Patients with severe COVID-19 infection 3.Patients with respiratory failure who need mechanical ventilation 4.Patients who cannot take drug orally 5.Inability or unwillingness to comply with study and/or follow-up procedures 6.Enrolled in other researches for treatment of COVID-19 infection.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The proportion of the patients becoming RT – PCR Negative after being positive for covid-19	baseline (day 0) and after 7th day (day 8) and after 10 days (day 11)

Secondary Outcome Measures

Name	Time	Method
Improvement in quality of life (SF-36 proforma will be used)	30 days follow up after stopping ayurvedic medication

Trial Locations

Locations (1)

All India Institute Of Ayurveda; 🇮🇳 South, DELHI, India

All India Institute Of Ayurveda

🇮🇳South, DELHI, India

Divya kajaria

Principal investigator

8826167515

divyakajaria@gmail.com