To know the efficacy of Amritabhallataka with virechana vs koshthshodhana in patients of Amavata (Rheumatoid Arthritis)
- Conditions
- Health Condition 1: M058- Other rheumatoid arthritis with rheumatoid factor
- Registration Number
- CTRI/2023/03/050182
- Lead Sponsor
- ALL INDIA INSTITUE OF AYURVEDA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients having the clinical manifestation of Amavata (RA) according to Ayurvedic classics
- Sandhishool (pain), shoth (swelling), sparshasahata (tenderness) and stabdhata
(stiffness),Vrishichikadansavata vedana(pain like scorpion sting), Agnimandya (poor
digestion) , Aruchi(anorexia), Gaurav(Feeling of heaviness of body),Utsaha Hani(lack of
interest),Mukha vairasya(Perverted taste).
2. Diagnosed cases of amavata (RA)
3. Patients willing to participate in the research study.
1) Patients with other systemic complications of RA like RHD, Rheumatic fever, pleural â??
pericardial disease.
2) Patients with poorly controlled Hypertension ( >160/100 mm of Hg)
3) Patients with Diabetes Mellitus {B.S. (F) > 126 mg% and / or B.S. (2 hr. PP) >200 mg%
OR HbA1c > 6.5%}
4) Patients diagnosed with other arthritis like gouty arthritis, tuberculous arthritis, etc.
5) Patients who are unable to walk without support and / or confined to wheel chair.
6) H/o hypersensitivity to any of the trial drugs or their ingredients.
7) Patients on prolonged ( > 6 weeks) medication with antidepressants, anticholinergic, etc. or
any other drugs that may have an influence on the outcome of the study.
8) Pregnant / lactating woman.
9) Patients who have completed participation in any other clinical trial during the past 6
months.
10) Patients allergic to any content of the drug.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method