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Clinical Study to evaluate the effectiveness of Linga chendooram in the management of Uthiravatha suronitham (Rheumatoid arthritis)

A pilot clinical trial to evaluate the effectiveness of Linga chendooram in the management of Uthiravatha suronitham (Rheumatoid arthritis) - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057492
Enrollment
10
Registered
2023-09-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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: Linga Chendooram: 65 mg twice daily with honey Oral route duration : 45 days

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Onset of arthritis after the age of 16 years Positive for rheumatoid factor (RF) Anti - CCP Either an erythrocyte sedimentation rate (ESR) of greater than 30 mm/hr OR C-reactive protein level greater than 1.0 mg/dl (normal less than 0.4) Diagnosis of Uthira Vatha Suronitham, as defined by fulfilling at least more than two articular involvements Minor Morning stiffness Willing to take study medication Willing to follow diet restriction Patients giving informed consent (Signed or oral witnessed, according to local regulations) before any Protocol specific procedures.

Exclusion criteria

Exclusion criteria: Uncontrolled Diabetes Mellitus Uncontrolled Hypertension Cardiac disease Renal disease Neurological disorders Pregnancy and lactation History of alcohol or substance abuse Active infection, or chronic or persistent infection that might worsen with immunosuppressive treatment Patients who have already participated in a new drug study in the past 3 months

Design outcomes

Primary

MeasureTime frame
Reduction of pain and swelling of the jointsTimepoint: Baseline and 12 th week

Secondary

MeasureTime frame
To study the clinical laboratory parameters related to RA RA Factor CRP ESR etcTimepoint: Baseline ad 12th wek

Countries

India

Contacts

Public ContactDr Janani Syamaroopa Jnanathapaswini

National Institute of Siddha,Tambaram,Chennai

drlakshmiramaswamy@gmail.com9025575185

Outcome results

None listed

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