A clinical trail to compare and study the effect of Panchatikta Ghruta Guggulu in the Management of Osteoarthritis in Postmenopausal Wome
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of kneeHealth Condition 2: M17- Osteoarthritis of kneeHealth Condition 3: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2024/08/071761
- Lead Sponsor
- KLE Ayurveda Hospital and Medical Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Subjects aged between 40 - 60 years.
2.Patients with classical presentations of Sandhigata vata and rajonivrutta stri will be selected irrespective of their religion and occupation.
3.Subjects fulfilling the diagnostic criteria & diagnosed previously (As per American college of Rheumatology (ACR) classification criteria for OA of the Knee).
4.Affected knee joint - Single or Both
5.Subject who submit a written informed consent.
6.One month after the completion of participation in any other clinical trial
1.Severe arthritis1.(KL grade IV)
2.Patients with RA, Gout, Osteoporosis and other musculoskeletal system disorders
3.Known cases of secondary OA due to tuberculosis (TB), syphilis, aids and leprosy
4.Gross disability like bedridden and confined to wheel chair
5.Patients with other major systematic disorders which interfere with the treatment will be excluded like uncontrolled DM
6.Patients with .Significant knee injury within past 6 months; presence of a rash or open 6.wound over the knee.
7.Use of NSAID’s, Analgesics, Intra articular steroid injections within the past period of 30 days
8.Patients with history of knee surgery or arthroscopy within the past year; knee replacement on study knee
9.Any other conditions which in the opinion of investigator will place the subject at risk or will influence the conduct of study or interpretation of results.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method