Health Condition 1: B359- Dermatophytosis, unspecified
Conditions
Interventions
None listed
Sponsors
Ayurvedic and Unani Tibbia College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient willing to participate in the trial and sign the consent form. 2. The patients between the age group of 18 to 60 years in either sex. 3. Patients of Dadru with features mentioned in subjective parameters. 4. Patient already taking modern medicine (Antifungals)& Local applications. 5. Patient having Potassium hydroxide (KOH) scrapping test positive
Exclusion criteria
Exclusion criteria: 1. Patients who were not willing for trial or fail to give consent. 2. Patients suffering from any other systemic illness,liver disorder, tuberculosis,bleeding disorder etc. 3. Pregnant and lactating women. 4. Patients taking antibiotic therapy for any systemic illness within 2 months. 5. H/O of hypersensitivity of any trial drug. 6. Allergic reaction to active substances of the leech such as hirudin,calin,hyaluronidase,egline,kollagenage,apyrase,destabilase,piyavit etc. 7. Patients with genetic and endocrinal disorder, chronic disorder like paralysis, cancer, renal failure, hepatic failure and IHD. 8. Patients having Tinea manuum and Tinea unguim. 9. Raktamokshana (jalaukavcharana)will not be done in Patients having diabetes mellitus.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in subjective parameters. Raga (Inflammation) Pidika (Eruption) Daha (Burning sensation) Rookshata (Dryness) Udgata mandal (Elevated lesion)Timepoint: 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment will be done clinically on basis of decrease in subjective parameters of dadruTimepoint: 12 weeks | — |
Countries
India
Contacts
Public ContactDr Sujata Yadav
Ayurvedic and Unani Tibbia college and hospital karol bagh New Delhi
Outcome results
None listed