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Role of abhyanga in osteoarthritis

Randomized controlled study to evaluate the efficacy of Shwadanshtradi taila Abhyanga in pain management of Janusandhigata Vata vis-à-vis knee osteoarthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045756
Enrollment
62
Registered
2022-09-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

None listed

Sponsors

SMBT Ayurveda College Dhamangaon Nashik
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of any gender, between age 35-70 years 2. Adults with persistent knee joint pain (shool/bhed) that worsens with use (prasaranakunchanyoh savedanaa) and morning stiffness lasting not more than half an hour i.e. suspected Osteoarthritis (OA) of Knee OR Patients diagnosed as unilateral or bilateral knee osteoarthritis and suffering from persistent knee joint pain but are either not taking regular anti-inflammatory/analgesic drugs or are not satisfied with drugs being taken and seeking change in treatment. 3. Patients willing to participate in the study

Exclusion criteria

Exclusion criteria: 1. Patients with Age 70 years 2. Grade > 3 of Kellgren and Lawrence scale for OA 3. Treatment with intra-articular injection of corticosteroids within a period of three month preceding study. 4. Patients having Fixed Flexion Deformity in knees or metallic implant in knee joint, or Obesity (BMI >30), or History of Acute Trauma 5. Patients who are unable to walk without aids or are Non-ambulatory 6. Patients diagnosed as Rheumatoid arthritis, inflammatory or infective arthritis [e.g., systemic lupus erythematosus (SLE)], Crystal arthritis (gout or pseudo-gout) or polyarthralgia, or Hemophilic arthropathy, or Bone and soft tissue tumours 7. Any other surgical or medical condition that severely limits subjects’ functional ability, or neurological conditions or Acute / sub-acute Infections

Design outcomes

Primary

MeasureTime frame
comparison of VAS score Timepoint: Baseline, 8th day and 14th day

Secondary

MeasureTime frame
a) WOMAC scale for functional disability measurement b) Clinical improvement in symptoms as per AyurvedaTimepoint: Baseline, 8th day and 14th day

Countries

India

Contacts

Public ContactDr Manoj Raut

Head of the department

dranilwagh@gmail.com9423212643

Outcome results

None listed

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