vitiligo. Vitiligo
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with symmetrical, unstable and non-segmental vitiligo
Exclusion criteria
Exclusion criteria: receiving any topical or systemic treatments during the last 3 months pregnancy, lactation history of any hypersensitivity to tacrolimus history of premalignant or malignant skin lesions photosensitivity, photo-mediated disorders, taking photo-sensitizing drugs concomitant radiotherapy, chemotherapy, or immunosuppressive therapy segmental or mucosal vitiligo
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Melanocyte stem cells location. Timepoint: before intervention and 2 months after intervention. Method of measurement: staining of the skin samples using monoclonal antibodies for the melanocytes and assessing the slides under a microscope. | — |
Secondary
| Measure | Time frame |
|---|---|
| The percentage of skin repigmentation. Timepoint: Before intervention and 2 months after intervention. Method of measurement: Using a quartile grading scale (grade 0, no repigmentation; grade 1, 1%-24%; grade 2, 25%-49%; grade 3, 50%-74%; grade 4, 75%-99%; grade 5, complete resolution). | — |
Countries
Iran (Islamic Republic of)
Contacts
Skin Research Center of Shahid Beheshti University of Medical Sciences