Clinical Comparative Study Of Nia VR ointment And Povidone Iodine Ointment in The Management Of Post Operative Transphincteric Anal Fistula Wound

Phase 2/3

Not yet recruiting

• Conditions: Disease of digestive system, unspecified. Ayurveda Condition: BAGANDARAH, (2) ICD-10 Condition: K928||Other specified diseases of the digestive system. Ayurveda Condition: BAGANDARAH,

• Registration Number: CTRI/2025/03/082986
• Lead Sponsor: National Institute Of Aayurveda

Brief Summary

Participants attending OPD and IPDof NIA Shalyatantra department satisfying the  selection criteria will be selected. All the participants who voluntarily agree to participate and provide informed written consent for participation will be recruIted in tHe study .

Total 60 participants will be selected after detail examination and divided in 2 groups of 30 patients as per study protocol.All procedures will be executed under aseptic precaution. Patient will be kept for 3 days in post operative days

assessment of the outcome will be on 7, 14 ,21 28 days Patient will be followed up on every 2 nd week after completion of trial for 2 months

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2025-03-17
• Study Start: 2025-04-30

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Patients of post operative partial fistulotomy (Anshik Bhedana) with Ksharasutra application between 20 to 60 yrs of age will be included in this study.
• Having no any other local or systemic ailment requiring active treatment.

Exclusion Criteria

Intersphincteric Extrasphinctericor Suprasphincteric anal fistula Patients with other concurrent diseases requiring active treatment.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Overall improvement to the wound	4 weeks
wound status will be assesed on the basis of subjective parameter i.e pain and gandha .Objective parameter stava and wound size .	4 weeks

Secondary Outcome Measures

Name	Time	Method
Change in the quality of life of the patient	12 week

Trial Locations

Locations (1)

NIA hospital; 🇮🇳 Jaipur, RAJASTHAN, India

NIA hospital

🇮🇳Jaipur, RAJASTHAN, India

Dipika Datir

Principal investigator

09665536904

dvd1998115@gmail.com