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A Comparative Study to evaluate the Effectiveness of Individualized Homoeopathic Treatment vs. Rhus Tox in Knee Osteoarthritis Patients Using the KOOS Scale as measure.

TWO ARM SINGLE BLINDED CONTROL TRIAL TO EVALUATE THE EFFECTIVENESS OF INDIVIDUALIZED HOMOEOPATHIC MEDICINE VIS- -VIS PATHOLOGICAL SIMILIA RHUS TOX IN CASES OF OSTEOARTHRITIS OF KNEE JOINT, USING THE KOOS SCALE AS MEASURE- A COMPARATIVE STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084032
Enrollment
140
Registered
2025-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: INDIVIDUALIZED HOMOEOPATHIC MEDICINE: GROUP A WILL RECIEVE INDIVIDUALIZED HOMOEOPATHIC MEDICINE. Intervention2: INDIVIDUALIZED HOMOEOPATHIC MEDICINE: GROUP A WILL RECEIVE INDIVIDUALIZED

Sponsors

P P SAVANI HOMOEOPATHIC MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: A. Age: Patients between the ages of 45 to 70 years. B. Diagnosis: Patients clinically diagnosed with osteoarthritis of the knee, confirmed through radiological findings based on the Kellgren-Lawrence grading scale (Grade I to III). C. Symptom Duration: Patients with a history of osteoarthritis symptoms (e.g., joint pain, stiffness) for at least 6 months. D. KOOS Score: Patients with moderate to severe knee function impairment, as reflected by the KOOS (Knee injury and Osteoarthritis Outcome Score). E. Consent: Patients willing to provide written informed consent and comply with the study procedures, including follow-ups. F. Ability to Participate: Patients physically and mentally capable of participating in assessments and reporting symptoms regularly.

Exclusion criteria

Exclusion criteria: A. Advanced Osteoarthritis: Patients with Kellgren-Lawrence Grade IV (end-stage OA) requiring surgical intervention such as total knee replacement. B. Comorbid Conditions: Patients with severe comorbidities, such as uncontrolled diabetes mellitus, cardiorespiratory diseases like congestive heart failure, uncontrolled hypertension, coronary artery disease, valvular heart disease, rheumatic heart disease, COPD, Allergic Asthma, and Chronic Asthma etc. , or any other chronic inflammatory diseases that could interfere with study results. The patient with controlled hypertension, non-progressive disease condition and only on anti-hypertensive drugs and not on any other steroidal or non-steroidal inflammatory drugs should be considered. C. Recent and Past Treatment History: Patients who are taking or who have taken following treatment in past 4 weeks; corticosteroids, NSAIDs, other disease-modifying osteoarthritis drugs (DMOADs), Physiotherapy, Ayurveda, Naturopathy and other forms of treatment. D. Surgical History: Patients with a history of knee surgery or joint replacement. E. Other Joint Diseases: Patients with concurrent rheumatologic diseases such as rheumatoid arthritis, gout, or ankylosing spondylitis. F. Pregnancy or Lactation: Female patients who are pregnant or breastfeeding. G. Non-compliance: Patients unwilling or unable to attend regular follow-ups or who do not adhere to treatment and assessment protocols.

Design outcomes

Primary

MeasureTime frame
There is no significant difference in the effectiveness of individualized homoepathic medicine and pathological similimum (Rhus tox) in managing osteoarthritis of the knee as measured by the KOOS scale.Timepoint: 9 MONTH

Secondary

MeasureTime frame
Individualized homoeopathic medicine is more effective than pathological similimum (Rhus tox) in managing osteoarthritis of the knee as measured by the KOOS scale. Timepoint: 9 MONTH

Countries

India

Contacts

Public ContactDR BHAVITA MALVI

P P Savani University

dr.bhavitamalvi@gmail.com9978198988

Outcome results

None listed

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