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Effect of Durvadi Taila and Povidone in Dustha Vrana

A Comparative Clinical Study of Durvadi Taila and Povidone Iodine in Dustha Vrana - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093151
Enrollment
60
Registered
2025-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: L089- Local infection of the skin and subcutaneous tissue, unspecified

Interventions

None listed

Sponsors

Dr Kritika Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients suffering from dushta vrana having clinical features like pricking and tearing type of pain foul smell pus discharge burning sensation itching were selected for the study Patients with wound size of less than 10cm 5cm 1cm Patients of either sex between the age group of 5 years and above Patients suffering from systemic diseases like uncontrolled diabetes mellitus tuberculosis etc will be include in the present study

Exclusion criteria

Exclusion criteria: Patients suffering from grave condition like malignant ulcer and other severe illeness like HIV HbsAg will be exclude Patients suffering from Dagdhavrana pressure ulcer Arterial ulcer Patients having pre gangrenous or gangrenous changes Patients suffering from osteomyelitis Vrana present on allmovable and highly movable joints Patients suffering from diabetic foot

Design outcomes

Primary

MeasureTime frame
Complete wound healingTimepoint: 1 month

Secondary

MeasureTime frame
Pain and Discharge reduction, Wound size reduction.Timepoint: 1 month

Countries

India

Contacts

Public ContactDr Kritika Sharma

Shri Babu Singh Jay Singh Ayurvedic Medical College and Hospital

ravivarma3856@gmail.com9036563856

Outcome results

None listed

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