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A Clinical trial in siddha for fistula with Panchapadana Chenduram and Meni thylam

A Pilot Clinical trial to determine the Efficacy of Siddha treatment with Panchapadana Chenduram and Meni thylam in the Management of Powthiram(Fistula in ano) - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061252
Enrollment
10
Registered
2024-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: K603- Anal fistula

Interventions

Intervention1: Panchapasana chenduram Meni thylam: Panchapasana chenduram 65 mg bd with palm jaggery and milk Meni thylam 5-10 ml HS warm water Control Intervention1: nil: nil

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient who will fulfil following criteria will be included in this study: 2. Age: 18 to 60 years. 3. Patients diagnosed with the condition of low anal fistula having single tract of length not more than 8 cm 4. Fistula patients of less than 3 years duration 5. Willingness of the patient to give blood and urine samples and cooperate by strictly complying with the medical advice of the research team. 6. Patients who had not undergone previous surgery for fistula

Exclusion criteria

Exclusion criteria: H/o Tuberculosis ?Uncontrolled metabolic disorders ? H/o Hepatitis B & C. ? H/o Haemophilia and bleeding disorders. ? H/o Pregnancy & Lactation. ? H/o Uncontrolled diabetes ? H/o coronary heart diseases and other cardiac ailments. ? H/o AIDS, Syphilis. ? H/o Crohn’s disease. ? High anal fistula and complicated fistula ? H/o Rectal prolapse ? H/o rectal carcinoma.

Design outcomes

Primary

MeasureTime frame
1. Number of patients achieved a Zero score of Peri Anal Disease Activity Index (PDAI). Timepoint: 90 days

Secondary

MeasureTime frame
Duration taken for healing will be analyzed and described with respect to the length of the tract and duration of the condition prior to the intervention.Timepoint: 90 days

Countries

India

Contacts

Public ContactDr K Jeyaradha

National Institute of Siddha

ramsnis@gmail.com9443178112

Outcome results

None listed

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