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To observe the effect of Siddha formulation Kabasura kudineer in COVID 19 patients

A randomized open labeled clinical study to compare the effectiveness of Kabasura kudineer and Vitamin-C Zinc supplementation in the management of asymptomatic SARS-CoV-2 patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025874
Enrollment
60
Registered
2020-06-15
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: Siddha medicine 30 â?? 60 ml twice daily orally Control Intervention1: Zinc and Vitamin C: Zinc -100 mg, Vit C â?? 60000 IU twice daily orally

Sponsors

Dean Government Theni Medical College
Lead Sponsor
Director General
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 and 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
1.Reduction in incidence of clinical symptoms like fever, cough and breathlessness. 2.Negative conversion of SARS-CoV-2 by 14 days 3.Reduction in Viral load of SARS-CoV-2 at the end of treatment (0, 7, 14 days) 4.Examine the levels of immune markers and inflammatory markers (IgG, IgM, IgA, Th1 (TNF-Alfa, IFN-gamma, IL2) Th2 (IL6, IL10) at the end of treatment (0, 7, 14 days) Timepoint: 14 days

Secondary

MeasureTime frame
1.Reduction in incidence of complications. 2.Reduction of in hospital time. 3.Laboratory markers 4.Adverse events/effects Timepoint: 14 days

Countries

India

Contacts

Public ContactDr C Anbarasi

Government Theni Medical College and Hospital

drsankararaj@gmail.com9965897075

Outcome results

None listed

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