Health Condition 1: L80- Vitiligo
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: •Cases more than 18 years of age •Patients who have given informed consent •Stability of lesions for at least 1 year •Presence of vitiliginous lesions over acral area not responding to any treatment modality
Exclusion criteria
Exclusion criteria: •Pregnant or lactating cases •Patients with a history of unstable vitiligo lesions •Cases with history of keloidal tendency •Patients with a history of Koebner phenomenon. •Patients not consenting to be a part of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of topical tofacitinib with microneedling vs topical 5 – fluorouracil with microneedling in cases of vitiligoTimepoint: 1 month | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the patient satisfaction in post-procedural settings using the vitiligo noticeability scaleTimepoint: 2 months;To determine the post procedural regimentation in both arms through the Pixel Assisted Regimentation Assessment in Vitiligo (PARAV) application.Timepoint: 1 month;To validate the Pixel Assisted Regimentation Assessment in Vitiligo (PARAV) application.Timepoint: 1 year | — |
Countries
India
Contacts
Dr.Vithalrao Vikhe Patil Foundations Medical College and Hospital