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Rheumatoid arthritis-A siddha classical drug Chitthira moolathi podi ( oral administration)

A prospective open labelled, non-randomized,phase II clinical trial of "CHITTHIRA MOOLATHI PODI" in the management of UTHIRAVATHA SURONITHAM(RHEUMATOID ARTHRITIS)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040076
Enrollment
40
Registered
2022-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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: CHITTHIRA MOOLATHI PODI (oral administration): Should be administrated orally twice a day after food along with hot water for 45 days dosage: 2 gm Control Intervention1: NIL: NIL

Sponsors

Dr V Nantha prasath
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: RA factor positive Anti ccp test positive CRP positive ANA test in few selected cases

Exclusion criteria

Exclusion criteria: Other joint diseases like osteoarthritis,seri negative spondylo arthritis,ankylosing spondylitis Infectious joint diseases like Tuberculosis, chronic poly arthritis in chickengunia viral infection Metabolic joint disease like gout Pregnancy and lactating mother Chronic renal and liver disease patients People with RA factor negative

Design outcomes

Primary

MeasureTime frame
In during treatment or after treatment reduction the following symptoms Pains in the more then 5 joints Morning stiffness Interphalangeal joints pain RA factor range Crp range Timepoint: 45 days

Secondary

MeasureTime frame
To evaluate the biochemical physico-chemical and phytochemical analysis of clinical trial drug To evaluate the antimicrobial activity of trial drug To evaluate the safety profile for acute and sub acute toxicity of the trial drug chitthira moolathi podi To evaluate pharmacological analysis of the clinical trial drug To evaluate Siddha parameters and modern parameters during the treatment of Uthiravatha suronitham with trial drug To evaluate the statistical analysis of the clinical trial drug Chitthira moolathi podi To evaluate the powder microscopic study and HTPLC of the trial drugTimepoint: 45 days

Countries

India

Contacts

Public ContactDr A Manoharan MD s Ph D

Government siddha medical college and hospital

komalaarumugam1@gmail.com9788122691

Outcome results

None listed

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