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use of VIRUNIL an Ayurvedic medicie as a supportive treatment in management of COVID-19.

Clinical evaluation of Virunil a standardized ayurvedic herbal compound as an adjuvant in management of COVID-19

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028635
Enrollment
150
Registered
2020-10-26
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 Health Condition 2: J99- Respiratory disorders in diseasesclassified elsewhere

Interventions

Intervention1: Virunil 500mg Capsules: 1500mg per day in divided doses (3doses per day) with water. for up to maximum of 10 days. Mode of Administration: Oral Control Intervention1: Standard Supporti

Sponsors

NRI ACADEMY OF SCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Voluntarily participating in the clinical study; fully understanding and being fully informed of the study and having signed the Informed Consent Form (ICF); willingness and capability to complete all the study procedures. Patient who are present in the stages of 1 and 2 of the COVID-19 disease.

Exclusion criteria

Exclusion criteria: 1. Patients with Auto Immune Disorders. 2. Patients with Co morbid conditions such as Diabetes Mellitus and Hypertension. 3. Patients Under any kind of Anti-Cancer medication, Immunosuppressants. 4. Patients who are under anti-platelet medication. 5. Patients with history of Organ Transplantation. 6. Patients with compromised pulmonary function. 7. Patients receiving antiviral drugs. 8. Pregnant and lactating mothers are also excluded from the study. 9. Any other condition, where investigators jeopardize the outcomes of the trials

Design outcomes

Primary

MeasureTime frame
The drug may reduce the hospital stay & inflammatory condition of COVID19 patientsTimepoint: At base line, 7th day and 10th day

Secondary

MeasureTime frame
Time from randomization to first time use of high flow supplemental oxygen/non-invasive ventilation/mechanical ventilation/ extracorporeal membrane oxygenationTimepoint: Randomization to hospital discharge (or day 28, which ever is earlier)

Countries

India

Contacts

Public ContactDr V Siva Prabodh

N R I MEDICAL COLLEGE AND GENERAL HOSPITAL

srivatsa.sivakrishna@gmail.com7075096010

Outcome results

None listed

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