A Comparative study on cauterization and internal medicine Arumuga Chenduram in management of Osteoarthritis
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecified
- Registration Number
- CTRI/2019/05/019141
- Lead Sponsor
- Ayothidoss Pandithar hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Patients suffering from primary osteoarthritis of knee joint.Signs and symptoms of Pain, tenderness, stiffness and crepitus in kneejoint. Patients willing to undergo radiological investigation (X RAY KNEE JOINT) and Laboratory investigations. Patients willing to sign the informed consent stating that he/she will Conscientiously stick to the treatment during 48 days but can opt out of the trial of his/her own conscious discretion.Patients willing to take photograph before and after suttigai therapy
Recent history of trauma, fracture , surgery of affected knee joint. Presence of local infection or skin disease on the proposed site of Suttigai.H/o Cardiac diseases,Uncontrolled Diabetes mellitus,Uncontrolled Hypertension, Rheumatoid arthritis, Chronic kidney disease, Pregnancy and lactation, Secondary OA due to tuberculosis(TB), syphilis, AIDS, leprosy, Septic arthritis, Gonococcal arthritis,Psoriatic arthritis. Patient with any other serious systemic illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome of the study is relieving pain and it will be assessed by KOOS KNEE SURVEY -Knee injury and Osteoarthritis Outcome Score (KOOS)- Before and after the treatment <br/ ><br> <br/ ><br>Timepoint: 45 days <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary outcome is assessed by comparing the clinical symptoms, clinical lab parameters and their quality of life before and after the treatment.Timepoint: 45 days