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A Clinical Study to assess the Effectiveness of Siddha treatment Therapeutic Purgation in the management of Patients with Santhuvatham (Polyarthritis)

A Three-Arm Randomized Parallel study to compare the effectiveness of Bethi Maruthuvam (Therapeutic Purgation) In vitiated Vatham with special reference to Santhuvatham (NSMC: Z26) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111649
Enrollment
90
Registered
2026-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: Arm 2: Therapeutic purgation : Agathiyar Kuzhambu-130 mg with 5 ginger juice Control Intervention1: Arm 1: Vatha decreasing drugs (Control): Amukkara Churanam 1 g twice daily with mi

Sponsors

Central Council for Research in Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed Santhuvatham patients Moderate to severe category based on V-Scale Age: 18 65 years

Exclusion criteria

Exclusion criteria: Renal disorders Patients with known cases of cardiovascular diseases and comorbid conditions (Diabetes& Hypertension) Pregnant and lactating women Paediatric and geriatric patients Rectal prolapse Bleeding from the urogenital tract or rectum

Design outcomes

Primary

MeasureTime frame
Primary Outcome Reduction in V-Scale score before and after intervention Secondary Outcomes Safety parameters Changes in intestinal microflora Timepoint: Primary Outcome Reduction in V-Scale score before and after intervention Secondary Outcomes Safety parameters Changes in intestinal microflora

Secondary

MeasureTime frame
Safety parameters Changes in intestinal microflora Timepoint: 1 year

Countries

India

Contacts

Public ContactDrRSusila

Siddha Clinical Research Unit

drsusilasiddha@gmail.com09865564621

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026