A study of blood letting and panchkarma procedure (oleation and sudation termed as Janu Basti) in the management of osteoarthritis knee pain.

Phase 2

• Conditions: Health Condition 1: M170- Bilateral primary osteoarthritis of knee

• Registration Number: CTRI/2022/09/045698
• Lead Sponsor: Shri Krishna Govt Ayurvedic College Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients aged 40-70 years.

Clinical signs, symptoms, and history of present illness suggestive of primary

osteoarthritis (grade 2and grade 3)

Exclusion Criteria

ââ? â?? Patients having age less than 40 year and more than 70 years.

ââ? â?? Patients having inconclusive diagnosis.

ââ? â?? Traumatic arthritis, rheumatoid arthritis, psoriatic arthritis, gouty arthritis and

other secondary osteoarthritis.

ââ? â?? Grade 1, Grade 4, Grade 518 type of primary osteoarthritis will be excluded.

ââ? â?? Patients having cardiac disease, renal disease, endocrine disorders and

malignancy will be excluded in the study to avoid overlapping of

symptomatology.

ââ? â?? Coagulopathy disorders will be excluded.

ââ? â?? Severe Anemia, pregnancy, any kind of noted drug allergy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare Raktavasechan (Jalaukavacharana) and Janu Basti in the management of Janu Sandhigata Vata (Osteoarthritis-knee jointsTimepoint: 1. Jalauka used for Blood Letting 4 times in 21 days <br/ ><br>0th day - 1st visit for blood letting <br/ ><br>7th day - 2nd visit for blood letting <br/ ><br>14th day - 3rd visit for blood letting 21th day - 4th visit for blood letting <br/ ><br> <br/ ><br>2. Janu Basti will be done once in a day for 21 days <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Changes in osteoarthritic features (pain, stiffness, inflammation and restricted movement) and improvement in life style along with other <br/ ><br>subjective parameters.Timepoint: Each patient has 21 days study period. <br/ ><br>Patient will be assessed weekly to check the improvement in subjective parameters.