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Effect of ayurveda interventions in the management of â??Amavataâ?? with special reference to Rheumatoid Arthritis.

Evaluation of Ayurvedic interventions in the management of â??Amavataâ?? W.S.R. to Rheumatoid Arthritis- a quasi interrupted time series design

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042860
Enrollment
30
Registered
2022-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Health Condition 1: M069- Rheumatoid arthritis, unspecified

Interventions

None listed

Sponsors

National institute of ayurveda deemed to be university jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to sign consent form for the clinical trial. 2. Patients between the age group of 18 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.

Exclusion criteria

Exclusion criteria: 1. Patients having severe joint deformities. 2. Patients suffering from paralysis. 3. Patients having any type of arthropathy such as Neoplasm of spine, Gout, Ankylosing spondylosis, Traumatic arthritis and Pyogenic osteomyelitis etc. 4. Patients having associated Cardiac disease, Tuberculosis, Diabetes mellitus, Malignant Hypertension, Renal Function Impairment, Hypothyroidism, Rheumatic Heart Disease etc. 5. Patients with extremely reduced joint space. 6. Pregnant women and lactating mother. 7. Patient taking disease modifying anti-rheumatic drugs (DMARDs) for rheumatoid arthritis.

Design outcomes

Primary

MeasureTime frame
Changes in DAS- 28 score.Timepoint: 56 Days

Secondary

MeasureTime frame
Changes in symptoms of Amavata, Improvement in quality of life and changes in CRP, RA Factor, Disability Index Score, other symptoms, Improvement in walking time, hand & foot grip.Timepoint: 56 Days

Countries

India

Contacts

Public ContactDR Nikita Sharma

National institute of Ayurveda Deemed to be University Jaipur

hari_mohan68@yahoo.co.in9461297017

Outcome results

None listed

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