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A clinical trial that will assess that effectivness of Rasanjanadi Lepa in treating Nadi Vrana (Pilonidal Sinus) through a randomised controlled trial.

A randomised controlled clinical trial to evaluate the efficacy of Rasanjanadi Lepa in mangament Of Nadi Vrana (Pilonidal Sinus) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082732
Enrollment
172
Registered
2025-03-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

None listed

Sponsors

Dr Sarvagya Pathak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group of patient 16 to 45 years. Patient diagnosed with Pilonidal Sinus & Abscess as per diagnostic criteria . Patient capable of reading , completing, and assigning the consent from participating in the study.

Exclusion criteria

Exclusion criteria: Presenting with dry & hard ulcer Presenting with Vatadhik Lakshan pregnant and lactating women Addiction to drugs and alcohol Abnormal bleeding from the wound using drugs that affect wound healing such as corticosteroids Using antibiotics prior to surgical intervention Not continuing the proposed treatment until the end of the study or request to leave the study History of severe allergy or anaphylactic shock caused by similar treatment Patient who has undergone organ transpiration Known case of connective tissue disease Known allergies to herbal drugs

Design outcomes

Primary

MeasureTime frame
Improvement in other symptoms or Pilonidal Sinus Wound dimension Depth of wound Wound excaudate quantity Bacterial load by culture & sensitivity test CRP Time period Wound volumetry Timepoint: 21 days

Secondary

MeasureTime frame
Improvement in other symptoms like painTimepoint: After analysing all the parameters the result will be assessed on the basis of symptomatic relief and improvement. Partially improvement after 7 days-patient get 40-60 percent relief from sign and symptoms. Improvement after 14 days- patient get 60-80percent relief from sign and symptoms. cured after 21 days -patient get 80-100 percent relief from sign and symptoms .

Countries

India

Contacts

Public ContactDr Krishnanand.C

Kunwar Shekhar Vijendra Ayurved Medical College and Research Centre , Gangoh, Saharanpur -247341

drkrishnanandc@gmail.com9360906457

Outcome results

None listed

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