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Effectiveness of constitutional homeopathic medicine in osteoarthritis

A prospective study to ascertain the effectiveness of constitutional homoeopathic medicines in cases of osteoarthritis in the age group of 35 to 65 years using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scale - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/095631
Enrollment
50
Registered
2025-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: M199- Osteoarthritis, unspecified site

Interventions

Intervention1: A PROSPECTIVE STUDY TO ASCERTAIN THE EFFECTIVENESS OF CONSTITUTIONAL HOMOEOPATHIC MEDICINES IN CASES OF OESTEOARTHRITIS IN AGE GROUP OF BETWEEN 35-65 YRS BY USING WESTERN ONTARIO McMAS

Sponsors

Sainath Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: Patients aged 35-65 years with a diagnosis of osteoarthritis (OA) based on clinical and radiological findings. 2. OA Diagnosis: Patients with a confirmed diagnosis of OA from radiological findings. 3. OA Severity: Patients with mild to moderate OA, as defined by the Kellgren-Lawrence grading system or the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). 4. Homoeopathic Treatment: Patients willing to receive homoeopathic treatment as part of the study.

Exclusion criteria

Exclusion criteria: 1. Severe OA: Patients with severe OA, as defined by the Kellgren-Lawrence grading system or WOMAC. 2. Other Rheumatic Diseases: Patients with other rheumatic diseases, such as rheumatoid arthritis, psoriatic arthritis, or gout. 3. Recent Injections or Surgery: Patients who have received corticosteroid injections or undergone surgery on the affected joint within the past 6 months. 4. Medications: Patients taking medications that may interfere with the study outcomes, such as: - Corticosteroids , Immunosuppressants , Opioids 5. Pregnancy or Lactation: Pregnant or lactating women. 6. Allergies or Sensitivities: Patients with known allergies or sensitivities to homoeopathic remedies. 7. Concurrent Treatment: Patients receiving concurrent treatment for OA, such as: - Acupuncture - Other alternative therapies 8. Cognitive or Psychiatric Impairment: Patients with significant cognitive or psychiatric impairment that may affect their ability to participate in the study.

Design outcomes

Primary

MeasureTime frame
Change in WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) total score from baseline to follow-up. WOMAC measures pain, stiffness, and physical function internationally validated, widely used in OA research.Timepoint: Baseline 15 days , 30 days , 45 days post treatment

Secondary

MeasureTime frame
Change in WOMAC domain scores (pain, stiffness, function) at 4, 8, and 12 weeks. Change in analgesic/NSAID requirement. Safety and tolerability of homoeopathic medicines.Timepoint: WOMAC Domain Scores (Pain, Stiffness, Physical Function) Time points: Baseline, 4 weeks, 8 weeks, 12 weeks (primary endpoint), and optionally 24 weeks (if you want longer-term follow-up). Use of Concomitant Analgesics / NSAIDs (frequency and dose reduction compared to baseline) Time points: Recorded at each follow-up visit (4, 8, 12 weeks). Adverse Events and Tolerability Time points: Monitored continuously; documented at every visit (4, 8, 12 weeks). Quality of Life (optional, e.g., SF-36 or EQ-5D if you plan to include it) Time points: Baseline and 12 weeks

Countries

India

Contacts

Public ContactKanani Manas Bhavikkumar

Rajkot Homoeopathic Medical College

hitarthmehtarhmc@paruluniversity.ac.in9825340073

Outcome results

None listed

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