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Evaluation of the Wound Cleansing Efficacy of Wound Fumigation done with Khadiradi Dhoop in Infected Wound: A Randomized Controlled Clinical Trial.

Evaluation of the Vrana Shodhana (wound cleansing) Efficacy of Vrana Dhoopan (wound fumigation) with Khadiradi Dhoop in Dushta Vrana (Infected Wound): A Randomized Controlled Clinical Trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102445
Enrollment
20
Registered
2026-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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 Aditya Pandya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient having any 3 of the following 5 clinical features of Dushta Vrana (Infected wound) will be considered for the study: Srava (Discharge), Durgandha (Foul Odour), Vedana (Pain), Kandu (Itching), Varna (Slough). Patients will be selected from an age group of 18 60 years of either Sex. Postoperative wound with symptoms of Dushta Vrana (Infected wound). Vrana (Wound) size: upto 8 x 8 cm (Length x Breadth).

Exclusion criteria

Exclusion criteria: Patients known case of systemic diseases like Uncontrolled Diabetes Mellitus. The patients with following conditions Malignancy Pregnancy Arterial ulcer, Venous ulcer, Marjolin s ulcer, Trophic ulcer, Leprosy.

Design outcomes

Primary

MeasureTime frame
Reduction in Wound Discharge assessed at 0 1st 3rd 5th and 7th day Timepoint: Reduction in Vrana Srava Wound Discharge assessed at 0 1st 3rd 5th 7th day

Secondary

MeasureTime frame
Reduction in Foul smell assessed at 0 1st 3rd 5th & 7th day Timepoint: Reduction in Foul smell assessed at 0 1st 3rd 5th 7th day;Reduction in Slough assessed at 0 1st 3rd 5th & 7th day Timepoint: Reduction in Slough assessed at 0 1st 3rd 5th & 7th day;Reduction in Pain assessed at 0 1st 3rd 5th & 7th day Timepoint: Reduction in Pain assessed at 0 1st 3rd 5th & 7th day;Reduction in Itching assessed at 0 1st 3rd 5th & 7th day Timepoint: Reduction in Itching assessed at 0 1st 3rd 5th & 7th day;Enhanced Granulation tissue formation assessed at 0 1st 3rd 5th & 7th day Timepoint: Enhanced Granulation tissue formation assessed at 0 1st 3rd 5th & 7th day

Countries

India

Contacts

Public ContactDr Aditya Pandya

Dr D Y Patil College of Ayurved and Research Centre Pimpri Pune

sanjaybabar2024@gmail.com9011035602

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026