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A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY of two formulations IN THE MANAGEMENT OF AMAVATA WITH SPECIAL REFERENCE TO RHEUMATOID ARTHRITIS

A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF SHOOLAPRSHAMANA CHOORNA AND HINGUTRIGUNA TAILA CAPSULE IN THE MANAGEMENT OF AMAVATA WITH SPECIAL REFERENCE TO RHEUMATOID ARTHRITIS

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046235
Enrollment
105
Registered
2022-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M049- Autoinflammatory syndrome, unspecified Health Condition 2: M049- Autoinflammatory syndrome, unspecified Health Condition 3: M368- Systemic disorders of connective tissue in other diseases classified elsewhere

Interventions

None listed

Sponsors

Dr Seeta MBiradar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENTS diagnosed as having Amavata on the basis of signs and symptoms that are typically diagnosed as classical symptoms and Rheumatoid Arthritis on basis of ACR CRITERIA FOR DIAGNOSING RHEUMATOID ARTHRITIS

Exclusion criteria

Exclusion criteria: patients suffering from complications of Aamavata Juveline RA Septic arthritis Rheumatic Heart Disease RA with involvement of other organs.

Design outcomes

Primary

MeasureTime frame
Subjective parameters Sandhi shoola Sandhi shotha Sparshasahatva Stabdata Angamarda Aruchi Alasya Objective parameters C-RP ESR Anti-CCP RA factor Assesment will be done on Pain Swelling Morning stiffness Tenderness Fever ESR score C-RP score DAS 28 score Disability Index Quality of Life Index SF36 by adapting standard methods of scoring.Timepoint: OBJECTIVE PARAMETERS C-RP ESR RA factor Anti-CCP ASSESSMENT CRITERIA Assessment will be made for clinical signs and symptoms & investigations Statistical analysis package of version 20 will be done by using chi-square/Fisher’s test for subjective parameters & students t test for objective parameters. SAMPLE SIZE 120PATIENTS 60 Patients in each group and treatment for 1month with follow up of 15days

Secondary

MeasureTime frame
Incidence of Amavata as per Age Sex Lifestyle will be made in Parul Institute of Ayurveda,Parul University Vadodara,GujaratTimepoint: 6months

Countries

India

Contacts

Public ContactDr Seeta MBiradar

Parul Institute of Ayurveda

shivani.gavande21706@paruluniversity.ac.in9420205131

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026