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Thokkanam in the management of Azhal Keel Vayu (Osteoarthritis of Knee joint) - A Pilot Study

An Open, Single Arm, Single Centric, Clinical Trial to Evaluate the Effectiveness of Thokkanam with Kunthrikka Thailam in the Management of Azhal Keel Vayu (Osteoarthritis of Knee joint) - A Pilot Study - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056676
Enrollment
15
Registered
2023-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Thokkanam with Kunthrikka Thailam: Thid is Physical manipulation therapy. Kunthriga thailam will be used as quantity sufficient. Session 1: Consecutively for 7 days Treatment holiday fo

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosed with primary OA as per clinical criteria of American College of Rheumatology for OA 2. Grade II or III KL grade radiographic changes in the knee 3. Willing to give specimen of blood for the investigation. 4. Permit to take photograph. 5. Willing to participate in trial and signing consent by fulfilling the condition of Proforma.

Exclusion criteria

Exclusion criteria: 1. Congenital abnormality, traumatic, infective condition or deformity subsequent to injury of knee joint which might have contributed to the development of secondary OA knee 2. Any previous history of surgical intervention on knee joint 3. Inflammatory arthritis (e.g., rheumatoid arthritis) 4. Grade IV OA on KL scale 5. History of Auto immune conditions 6. A rash or open wound over the knee

Design outcomes

Primary

MeasureTime frame
Reducing pain, stiffness & physical function disability domains of Azhal keel vayu (Osteoarthritis of Knee joint) through Western Ontario & McMaster Universities Osteoarthritis IndexTimepoint: 21 Days

Secondary

MeasureTime frame
Improvement in Quality of Life of the patients using SF-36 QuestionnaireTimepoint: 21 Days;Improvement in range of motions of knee joint in degree using standard goniometric measurementsTimepoint: 21 Days;Reduction in the level of pain through Visual analog scale Timepoint: 21 days;Time taken to walk 50 feet pathTimepoint: 21 Days

Countries

India

Contacts

Public ContactDr Subhashri R

National Institute of Siddha

mahasiddha2009@gmail.com9840417565

Outcome results

None listed

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