Health Condition 1: M170- Bilateral primary osteoarthritis of knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients having symptoms of pain in single or both knee joints, swelling, tenderness, stiffness, crepitation and restricted movements Patients who are willing to give blood samples for laboratory investigation Patients who are willing to take x ray before and after treatment Willing for admission in IPD for 48 days or wiling to attend OPD regularly Patients who are willing to participate in this study with knowledge of potential risks and who are willing to sign the informed consent
Exclusion criteria
Exclusion criteria: Cardiac disease Rheumatoid and other types of arthritis Pregnant women and lactating mothers Trauma, fracture and ligament injury Patients with any other serious illness Benign and malignant neoplasm Immuno compromised patients Dermatological issues
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of changes from baseline in universal pain assessment scale score at day 48 between Group I (Pattru External therapy) and Group II (Medicine and Pattru external therapy) Comparison of efficacy in patient Group I and Group IITimepoint: 48 Days | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of quality of life by universal pain score scale Assessment of safety parametersTimepoint: 48 Days | — |
Countries
India
Contacts
Government Siddha Medical College and Hospital