Health Condition 1: L80- Vitiligo
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients with stable (no new lesions or increase in size of pre-existing lesions in the last 3 months or more) / repigmenting non-segmental (generalized or acrofacial) vitiligo of any extent, irrespective of ongoing local treatment (including topical immunomodulators, topical photochemotherapy, hand-held NbUVB, excimer light), and off-systemic treatments or whole body phototherapy for at-least 4 weeks
Exclusion criteria
Exclusion criteria: Patients with active vitiligo (in the last 3 months) or unsure disease course Patients with stable non-segmental vitiligo of less than 3 months Patients on systemic treatment or phototherapy in the last 4 weeks Pregnant or lactating females Patients with concurrent skin or systemic inflammatory disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To identify serum biomarkers to predict future disease activity in patients with stable/repigmenting non-segmental vitiligo at 3-12 months follow-upTimepoint: 0, 3, 6, 9, 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To identify tissue biomarkers to predict future patch activity in patients with stable/repigmenting non-segmental vitiligo at 3-12 months follow-up 2. To identify dermoscopic features to predict future patch activity in patients with stable/repigmenting non-segmental vitiligo at 3-12 months follow-up 3. To identify clinical features to predict future disease activity in patients with stable/repigmenting non-segmental vitiligo at 3-12 months follow-up 4. To assess the longitudinal change in serum biomarkers 5. To correlate serum biomarkers with vitiligo extent, type and activity 6. To compare tissue biomarkers between acral and non-acral vitiligo patches Timepoint: 0, 3, 6, 9, 12 months | — |
Countries
India
Contacts
All India Institute of Medical Sciences