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Effectiveness of Siddha medicine, Kabasura kudineer and vitamin c-zinc supplementation in the management of Mild COVID 19 patients.

A prospective, single centre, randomized open labelled comparative clinical study to evaluate the effectiveness of Siddha medicine, Kabasura kudineer and vitamin c-zinc supplementation in the management of asymptomatic COVID 19 patients.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025215
Enrollment
50
Registered
2020-05-16
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: Kabasura Kudineer: 60 ml bd for 14 days Control Intervention1: Vitamin C, Zinc supplementation: Vitamin C - 60000IU OD for 14 days Zinc supplementation - 100mg od for 14 days

Sponsors

Dean
Lead Sponsor
Central Council for Research in Siddha
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Laboratory confirmed COVID-19 without symptoms 2.Consenting to participate in the study and sign the informed consent

Exclusion criteria

Exclusion criteria: 1.Patient with co morbid conditions like DM, HT, BA 2.Patients with severe primary respiratory disease or other pathogenic microbial pneumonia that needs to be identified with COVID-19 3.Pregnant and mothers, those who have a pregnancy plan. 4.Patients with other systemic malignant diseases such as malignant tumors, mental illnesses, etc., which the researchers consider unsuitable for participation in the study 5.People who have been allergic to Siddha medicine or intolerant to taking medicine 6.Patients participating in other COVID-19 clinical trials

Design outcomes

Primary

MeasureTime frame
Reduction in incidence of clinical symptoms of COVID 19 Negative conversion of SARS-CoV-2 Reduction in Viral load of SARS-CoV-2 at the end of treatment Examine the levels immune markers and inflammatory markersTimepoint: 14 days

Secondary

MeasureTime frame
Reduction of in hospital time adverse events/effects Siddha Udaliyal assessment Siddha Uyir thathukkal and udal thathukkal assessmentTimepoint: 14 days

Countries

India

Contacts

Public ContactDr C Anbarasi

Siddha Central Research Institute

drnatarajan78@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 25, 2026