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Effectivenes of Siddha Supplement MAM Granules in the Management of Pre Symptomatic COVID 19 patients

An Open labelled RCT to Evaluate the Efficacy and Safety of Siddha Supplement (MAM Granules) along with Standard Allopathy Treatment in the management of RT PCR Positive Pre Symptomatic COVID 19 patients - MAMSRCT

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031420
Enrollment
60
Registered
2021-02-19
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: Siddha MAM Granules: 2gms with milk morning and night after food for 14 dayswith Standard Allopathy Care (Vit C & Zinc) Control Intervention1: Standard Allopathy Care (Vit C & Zinc): mi

Sponsors

Central Council for Research in Siddha
Lead Sponsor
Government Institute of Medical Sciences GIMS
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Laboratory Confirmed COVID â?? 19 with Asymptomatic Patient (as per ICMR Guidelines) 30 Patients in each group 2. Aged 18-65 years 3. Consenting to participate in the study and sign the informed consent

Exclusion criteria

Exclusion criteria: 1. Patients with severe primary respiratory disease or other pathogenic microbial pneumonia 2. Patient with Uncontrolled DM (>= 350 mgs Fasting Sugar) Severe HT (180/120 mmHg as per JNC 8 Guidelines), Chronic BA (>= 5 years Based on Clinical History), Renal Dysfunction (Known CKD >= 5 years eGFR Stage >= 3 as per NKA guidelines) 3. Pregnant and Lactating mothers 4. People who have history of allergic to Siddha medicine or intolerant to taking medication 5. Patients participating in other COVID-19 clinical trials 6. Patients already went under COVID 19 vaccination

Design outcomes

Primary

MeasureTime frame
Reduction in incidence of clinical symptoms like fever, cough and breathlessness Negative conversion of SARS CoV - 2 by 14 days Reduction in Viral load of SARS CoV â?? 2 at the end of treatment Effect of drugs inflammatory markers (IL6) and other Immunity Markers at the end of treatment. Timepoint: 14 days

Secondary

MeasureTime frame
Reduction in incidence of complications (ARDS, other systematic complications) Laboratory markers (Hematological & Bio â?? Chemical Markers) Adverse events/effects Siddha-based measurements Siddha Udaliyal assessment by using YI Tool Timepoint: 14 Days

Countries

India

Contacts

Public ContactDr Anurag Srivastava

Government Institute of Medical Sciences GIMS

dranurag23@gmail.com7303884221

Outcome results

None listed

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