Health Condition 1: L80- Vitiligo
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients/ Legally authorized representative (LAR) providing written informed consent towards participation in the study 2. All patients of Vitiligo with disease stability for last three (3) months 3. Patients with Vitiligo bilaterally symmetrical in distribution 4. Patients unresponsive to medical treatment or photo therapy 5. Patients older than 18 years
Exclusion criteria
Exclusion criteria: 1. Vitiligo involving head and neck, face, intertriginous areas, hands and feet 2. Pregnant and Lactating female 3. Patients with Haemoglobin 4. Patients with Platelet count 5. Patients with bleeding diathesis 6. Patients with active infection 7. Patients with history of Keloid/ Hypertrophic scars 8. Patients with history of Koebnerization 9. Patients with Chronic liver disease 10. Patients on chemotherapy, anti-coagulation therapy and antiplatelet agent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Vitiligo European Task Force Assessment (VETF) 2. Vitiligo Area Scoring Index (VASI)Timepoint: Baseline, every 2 weeks of treatment and after 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Scoring system of Repigmentation 2. Patient SatisfactionTimepoint: Baseline, every 2 weeks of treatment and after 3 months | — |
Countries
India
Contacts
CALCUTTA SCHOOL OF TROPICAL MEDICINE