FindTrial
Sign In

A CONTROLLED CLINICAL STUDY TO EVALUATE THE EFFICACY OF PATOLADI TAILA ON POST OPERATIVE AGNIDAGDHA VRANA

A CONTROLLED CLINICAL STUDY TO EVALUATE THE EFFICACY OF PATOLADI TAILA ON POST OPERATIVE AGNIDAGDHA VRANA

Status
Unknown
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033160
Enrollment
60
Registered
2021-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: L84- Corns and callosities Health Condition 2: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere

Interventions

Intervention1: PATOLADI TAILA: EACH PATIENTS OF KADARA WILL BE SUBJECTED TO AGIKARMA AND APPLICATION OF PATOLADI TAILA OVER THE DAGDHA VRANA ONCE A DAY FOR 14 DAYS Control Intervention1: POVIDONE IODI

Sponsors

ASHOK
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed patients of corn. Patients of age group 16-70 years will be selected irrespective of sex, occupation, religion & socio-economic status. In patients who are fit for Agnikarma

Exclusion criteria

Exclusion criteria: Patients Contraindicated for Agnikarma. Patients with Systemic disorders. Patients with infective conditions like HIV and HbsAg will be excluded. Pregnant women

Design outcomes

Primary

MeasureTime frame
Rough Tough Yellowing patch of lumpy skin on plantar surface and painTimepoint: 45 DAYS—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr POONAM

ALVAS AYURVEDA MEDICAL COLLEGE AND HOSPITAL

dmbg2004@gmail.com9686751182

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026