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To study the effect of Vyaghradi Kashay tablet on COVID-19 patients

An interventional, single arm study to observe and assess the effectiveness of â??Vyaghradi Kashaya Tabâ?? in preventing the progression of severity in asymptomatic, mild to moderate COVID-19 cases.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028570
Enrollment
30
Registered
2020-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere

Interventions

Intervention1: Vyaghradi Kashay Tablet: Drug- Vyaghradi Kashay Tablet Dose : One tab(500mg)three times a day with luke warm water Route -Oral Duration - 7 days (Initially). If RTPCR Not negative in 7

Sponsors

Ministry of AYUSH Govt of India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: People who have been tested positive to be infected with SARS-CoV2 virus and presenting with no symptoms or with mild to moderate symptoms. All the patients of age group 18-65 yrs All those who are willing to give written consent for participation in the study

Exclusion criteria

Exclusion criteria: COVID patients with symptoms classified as severe or critical. Persons with severe primary respiratory disease or other pneumonia Pregnant and lactating women Persons with serious complications of diseases such as cancer, heart disease, stroke, disabilities, mental illnesses, etc., and who are considered to be excluded from the study as evaluated by the investigators COVID-19 positive cases participating as subjects in the interventional arm of other COVID-19 clinical trials.

Design outcomes

Primary

MeasureTime frame
Time taken to be tested negative for SARS-CoV2 in RT-PCR. To Assess the effect of drug in preventing the progression of severity of symptoms.Timepoint: a)RT PCR 7th and 14th Day b)Assessment of clinical recovery at baseline, Daily 7-14 days

Secondary

MeasureTime frame
Secondary outcome- To assess the effect of Vyaghradi Kwath Tab on blood parameters specific to Covid-19. Timepoint: 08-15 days

Countries

India

Contacts

Public ContactDr Nitin Jindal

A and U Tibbia College and Hospital Govt of NCT of Delhi

manoj_1873@yahoo.co.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026