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To see the effect of nirgundi kwath and a herbal formulation in primary osteoarthritis of knee joint

Not yet recruiting
Conditions
Osteoarthritis of knee, unspecified. Ayurveda Condition: SANDHIGATAVATAH,
Registration Number
CTRI/2022/07/043964
Lead Sponsor
Patanjali Bhartiya Ayurvigyan Evum Anusandhan Sansthan Haridwar
Brief Summary

In this trial we are selecting the patients of Primary osteoarthritis of knee in which we will do intervention in two groups (20 patients in each). In one group, we will intervene our ayurvedic preparation(Nirgundi kwath and a herbal formulation tablet) whereas in other group placebo will be given to the patients. Assessment should be done on the basis of assessment done before treatment, during. Follow up and post treatment as discussed earlier.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria
    1. Patient will be selected irrespective of Sex and socio-economic status. 2. Patients have fulfilling criteria for diagnosis of Janu Sandhigatavata such as Sandhishoola, Sandhishotha, Sparshashatva, Sandhisphutan. 3. Age.
  • 40 to 65 years. 4. Patient with Controlled Diabetes. 5. Patient falling in Grade 1 and Grade 2 of Kellgren–Lawrence radiographic grading scale of osteoarthritis.
Exclusion Criteria
  • Knee Osteoarthritis secondary to other conditions like Trauma, Fractures, Tuberculosis, malignancy, HIV, Cardiac disease, Neurological disorders, associated with Janu Sandhigatavata.
  • Patient with total knee joint replacement or complete loss of articular cartilage.
  • Patients having other systemic disorders which might interfere in the present study.
  • like Amavata (Rheumatoid Arthritis), Gout (Vatarakta), Severe bursitis.
  • Pregnant and lactating women.
  • Patient falling in Grade 3 and 4 of Kellgren–Lawrence radiographic grading scale of Osteoarthritis.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
X Ray of involved knee joint (Antero Posterior and Lateral View)-Before intervention of the treatment
2. Radiography-I To diagnose the patients (at or before day 0) at the time of inclusion.Before intervention of the treatment
3. Radiography-II To be compared with Radiography-I at the time of final assessmentBefore intervention of the treatment
Secondary Outcome Measures
NameTimeMethod
X Ray of involved knee joint (Antero Posterior and Lateral View)-2. Radiography-I To diagnose the patients (at or before day 0) at the time of inclusion.

Trial Locations

Locations (1)

Patanjali Ayurveda Hospital

🇮🇳

Hardwar, UTTARANCHAL, India

Patanjali Ayurveda Hospital
🇮🇳Hardwar, UTTARANCHAL, India
Dr Lata Arya
Principal investigator
6395353273
aryagunjanlata@gmail.com

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