Skip to content

Effect of Shathi-Vishwaushadhi tablets in patients with rheumatoid arthritis (Amavata) and its impact on inflammation (C-reactive protein)

Single arm clinical study to assess Samprapti bhang of Amavata by Shathi-Vishwaushadhi Vati with special reference to C-reactive protein - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105282
Enrollment
65
Registered
2026-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

LRP AYURVED MEDICAL HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with classical signs and symptoms of Amavata such as: Sandhishool (joint pain) Sandhishotha (joint swelling) Sandhistabdhata (joint stiffness) Sparsha asahatva (joint tenderness) Patients diagnosed with Amavata (Rheumatoid arthritis). Patients having raised C-reactive protein (CRP) levels between 10 50 mg/L. Duration of illness up to 1 year. Patients aged between 20 60 years. Patients of either sex willing to participate and sign informed consent.

Exclusion criteria

Exclusion criteria: Patients aged below 20 years and above 60 years. Pregnant and lactating women. Patients suffering from other autoimmune or infectious arthritic disorders such as: Systemic lupus erythematosus Psoriatic arthritis Syphilitic arthritis Immunocompromised patients. Patients unwilling to participate or sign informed consent.

Design outcomes

Primary

MeasureTime frame
Change in serum C-reactive protein (CRP) levels (mg/L) before and after treatment with Shathi-Vishwaushadhi VatiTimepoint: At baseline, 4 weeks & 8 weeks

Secondary

MeasureTime frame
Reduction in Sandhishool (joint pain score)Timepoint: Day 0, Day 3, Day 5 and Day 7;Reduction in Sandhistabdhata (joint stiffness score)Timepoint: Day 0, Day 3, Day 5 and Day 7;Reduction in Sparsha asahatva (joint tenderness score)Timepoint: Day 0, Day 3, Day 5 and Day 7;Reduction in Sandhishotha (joint swelling in cm)Timepoint: Day 0 and Day 7;Improvement in grip strength (mmHg)Timepoint: Day 0 and Day 7;Improvement in functional activity scoreTimepoint: Day 0, Day 3, Day 5 and Day 7

Countries

India

Contacts

Public ContactDr Shubhangi Dahiphale

L.R.P AYURVEDIC MEDICAL COLLEGE, HOSPITAL, POST GRADUATE INSTITUTE AND RESEARCH CENTER

drabhay1988khot@gmail.com9172710091

Outcome results

None listed

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