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To know the efficacy of Amritabhallataka with virechana vs koshthshodhana in patients of Amavata (Rheumatoid Arthritis)

Phase 2
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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