None listed
Conditions
Interventions
None listed
Sponsors
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
| Measure | Time 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
| Measure | Time 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
Kunwar Shekhar Vijendra Ayurved Medical College and Research Centre , Gangoh, Saharanpur -247341