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Siddha Intervention for Osteoarthritis

A randomized controlled three arm clinical trial on the of effectiveness Mudakku Vatha Ilagam (MVI) and Varmam Therapy in Midlife population afflicted by Azhal Keel Vayu (AKV Knee-Osteoarthritis).

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/04/018752
Enrollment
54
Registered
2019-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: Mudakku Vatha Ilagam: 5 gms - Oral dose Twice a day with hot water After food intake Control Intervention1: Varmam Therapy 1.MuttuVarmam 2.SanthiVarmam 3.MozhiPoruthuVarmam 4.PathaipuVa

Sponsors

Central Council for Research in Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Sex – Both sex 2. Patients with Primary Osteoarthritis - knee joints (single or both knees). 3. Swelling in the Knee Joints 4. Joint stiffness 5. Restricted movements of joints. 6. Crepitus of joints. 7.Patients with WOMAC Score = 25 = 72

Exclusion criteria

Exclusion criteria: 1.Age less than 40 years or more than 60 years. 2.Patients with Diabetes/Hepatic failure/Renal failure. 3.History of bony or soft tissue injury to knee joint/ surgical interventions 4.Patients having Rheumatoid arthritis, Gout, Viral fever (Chikungunya) and Psoriatic arthritis. 5.Patients who are taking any form of steroids.

Design outcomes

Primary

MeasureTime frame
1.Safety of the study drug will be assessed by using following parameters: CBC, HB, PCV, LFT, RFT, Diabetic profile, Lipid profile and Urine routine on 0 day and 31st day. 2.Efficacy of the trial drug will be assessed by WOMAC 3.1 INDEX on 0 day, 31st day and 90th day.Timepoint: 0 day - Before inclusion of Trial . 31st day - After Successful completion of Trial. 90th day - Trial Follow-up

Secondary

MeasureTime frame
Improvement in the quality of life of AKV patients will be evaluated through OAKHQOL index on 0 day, 31st day and 90th day.Timepoint: 0 day - Before inclusion of Trial . 31st day - After Successful completion of Trial. 90th day - Trial Follow-up

Countries

India

Contacts

Public ContactDr S Shunmugaram

Siddha Regional Research Institute

dr.s.s.ram28@gmail.com8608533131

Outcome results

None listed

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