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A Clinical trial to study the effect of the drug Chanthirothaya Mathirai in management of patients having Rheumatoid Arthritis(Uthiravatha Suronitham)

Phase II Non-Randomized Open Clinical Evaluation of Siddha Medicine Chanthirothaya Mathirai for the management of Uthiravatha Suronitham (Rheumatoid Arthritis)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037553
Enrollment
40
Registered
2021-10-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M059- Rheumatoid arthritis with rheumatoid factor, unspecified

Interventions

Intervention1: CHANTHIROTHAYA MATHIRAI: 360 mg of Chanthirothaya Mathirai is administered twice a day with Indhuppu legiyam for 48 days Control Intervention1: NIL: NIL

Sponsors

Government Siddha Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age limit of 20-55 years Anti Cyclic Citrullinated Peptide(AntiCCP)-5ml or more and RA positive H/O Morning stiffness for more than 1 hour Multiple joint involvement Symmetreical Arthritis Rheumatoid Nodules

Exclusion criteria

Exclusion criteria: H/O Rheumatic fever H/O Psoriatic Arthropathy H/O Reiters Arthritis H/O Systemic Lupus Erythematous H/O Sjogrens syndrome H/O Progressive Systemic Sclerosis H/O Any other serious systemic Illness Pregnant women, Lactating Mothers

Design outcomes

Primary

MeasureTime frame
Primary outcome is mainly assessed by reduction in clinical symptoms measured by Universal pain Assessment Scale(Visual Analogue Scale)Timepoint: 48 days

Secondary

MeasureTime frame
Secondary Outcome is assessed by comparing the safety parameters before and after treatmentTimepoint: 48 days

Countries

India

Contacts

Public ContactDr Sudhaadevi PV

Government Siddha Medical College

chittu758@gmail.com9444177230

Outcome results

None listed

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