To study the effect of Pavanari Rasa for pain management in Amavata.
- Conditions
- Health Condition 1: M04-M04- Autoinflammatory syndromes
- Registration Number
- CTRI/2023/07/055293
- Lead Sponsor
- ational Institute of Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients willing to sign consent form for the clinical trial.
2.Patients between the age group of 25 to 60 years, irrespective of sex and socio-economic status.
3.Patients having signs and symptoms of â??Amavataâ?? (Rheumatoid Arthritis)
4.Patients fulfill the criteria of ACR / EULAR 2010 criteria (American College of Rheumatology /European League Against Rheumatism)
5.Patients with chronicity of less than 5 years.
1.Patients having severe joint deformities.
2.Patients having age < 20 years & > 60 years .
3.Patients suffering from paralysis.
4.Patients having any type of arthropathy such as Neoplasm of spine, Gout, Ankylosing spondylosis, Traumatic arthritis and Pyogenic osteomyelitis etc.
5.Patients having associated Cardiac disease, Tuberculosis, Diabetes mellitus, Malignant Hypertension, Renal Function Impairment, Hypothyroidism, Rheumatic Heart Disease etc.
6.Patients with extremely reduced joint space.
7.Pregnant women and lactating mother.
8.Patient taking disease modifying anti-rheumatic drugs (DMARDs) for rheumatoid arthritis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in Pain score.Timepoint: 14 days
- Secondary Outcome Measures
Name Time Method Changes in symptoms of Amavata, Improvement in quality of life and changes in DAS-28 score, CRP, RA Factor, Disability Index Score, other symptoms, Improvement in walking time,hand &foot grip.Timepoint: 30 days