Health Condition 1: L80- Vitiligo
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: Nil
Sponsors
Department of Dermatology
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with clinical diagnosis of segmental or non segmental vitiligo 2. Patients with active disease 3. Patients initiated on medical management
Exclusion criteria
Exclusion criteria: 1. Patients with stable disease 2. Patients who receive phototherapy or surgical management 3. Patients who did not give consent for participation in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To sequentially determine the dermatoscopic features of vitiligoTimepoint: Baseline, 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks, 24 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To correlate dermatoscopic features with disease activity assessed by means of VIDA and VASI 2. To correlate dermatoscopic features of repigmentation with treatment modality usedTimepoint: 24 weeks | — |
Countries
India
Contacts
Public ContactVinay K
Department of Dermatology, PGIMER, Chandigarh
Outcome results
None listed