Health Condition 1: null- Patients suffering from Amavata.
Conditions
Interventions
Intervention1: Group B Amavatari Rasa without mercury
: 125 mg thrice in a day
anupana luke warm water
duration 28 days
14 days follow up
Control Intervention1: Group A Amavatari Rasa classical: 125
Sponsors
Institute for Post Graduate Teaching and Research in Ayurveda
Eligibility
Inclusion criteria
Inclusion criteria: 1 Patients having classical symptoms of Amavata will be taken from OPD and IPD of Department of Rasa Shastra and Bhaishajya Kalpana IPGT&RA Jamnagar Angamarda Bodyache Aruchi Anorexia TrishnaThirst Alasya Laziness Gauravam Heaviness Jvara Fever Apaka Indigestion ShunataAnganam Swelling over all body 2 Age of patients will be between 20 to 50 years 3 Modern Criteria for the diagnosis of Rheumatoid arthritis In addition to the classical symptomatology of Amavata as emphasized in Ayurvedic classics Presence of any four of the following criteria based on the revised criteria of American college of Rheumatology 1987 1 Morning stiffness lasting for more than one hour 2 Arthritis of three or more joints 3 Arthritis of hand joints 4 Symmetrical arthritis 5 Presence of rheumatoid nodules 6 Presence of rheumatoid factor 7 Typical Radiographic changes of Arthritis on PA view of Hand and wrist radiograph that must include erosions and unequivocal decalcification adjacent to involve joints Criteria 1 2 3 and 4 must be present for the duration of six weeks or more
Exclusion criteria
Exclusion criteria: Patients having chronic complications like severe crippling deformities and other forms of arthritis like Ankylosing Spondylosis Osteo Arthritis etc Known cases of TB DM HTN cardiac disease liver disease etc Age less than 20 years and more than 50 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in the signs and symptoms before and after treatment. The Assessment Criterion based on the guidelines provided in the Clinical Research Protocol of CCRAS will be considered for the sameTimepoint: 28 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement in the signs& symptoms before and after treatment. The Assessment Criterion based on the guidelines provided in the Clinical Research Protocol of CCRAS will be considered for the sameTimepoint: 28 days | — |
Countries
India
Contacts
Public ContactProf P K Prajapati
IPGTRA GAU Jamnagar
Outcome results
None listed