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Role of Abhadya Churna and Shatyadi Kwatha in management of Amavata (Sandhi shola).

A COMPARATIVE CLINICAL STUDY OF ABHADYA CHURNA AND SHATYADI KWATHA ON AMAVATA IN THE PURVIEW OF LANGHANAM SWEDANAM TIKTAM DIPANANI KATUNI CA Chakradutta 25/1

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040636
Enrollment
30
Registered
2022-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Health Condition 1: M056- Rheumatoid arthritis with involvement of other organs and systems

Interventions

Intervention1: Group A -Abhadya Churna: Group A-15 Clinically diagnosed and registered patients of â??Amavataâ?? will be treated by â??Abhadya Churnaâ?? in the dose of 3gm two times in a day (morning

Sponsors

National Institute of Ayurveda 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 with clinical feassture of Amavata as described in Madhavniadan. 4. Patients with chronicity of less than 10 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 woman and lactating mother. 7. Chronicity of Amavata more than 10 years.

Design outcomes

Primary

MeasureTime frame
Changes in the values of Rheumatoid Factor CRP and ESR.Timepoint: 60 days

Secondary

MeasureTime frame
Secondary outcome measures Change in the objective / laboratory parameters and subjective parameters 1. Angamarda (Bodyache) 2. Aruchi (Anorexia) 3. Jwara (Fever)Timepoint: 60 days

Countries

India

Contacts

Public ContactDr Sangita Choudhary

National Institute of Ayurveda,Jaipur

guptadr.nisha@gmail.com9828087640

Outcome results

None listed

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