Comparative Study of Microneedling With Topical Minoxidil 5% ± NB-UVB in Stable Vitiligo"
Phase 2 – studying effectiveness and dosage
Conditions:
Vitiligo - Macular Depigmentation
Sponsor: Sohag University
trial.available_in:
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Overview
This study is a randomized controlled trial comparing microneedling with topical minoxidil 5% versus microneedling with minoxidil combined with NB-UVB phototherapy in stable vitiligo.
It aims to evaluate both clinical and histopathological outcomes in 30 patients with non-segmental stable vitiligo.
Vitiligo is a chronic depigmenting disorder caused by melanocyte destruction with significant psychosocial impact.
The study also investigates immunohistochemical changes, particularly Wnt/β-catenin signaling expression in lesional skin.
The combination therapy is expected to enhance repigmentation by improving melanocyte activation, drug delivery, and angiogenesis
Who can participate
Inclusion Criteria:
* Patients with stable non-segmental vitiligo (no new lesions, and no enlargement of existing lesions).
Patients of both sexes Age 16 years or older
Exclusion Criteria:
Active vitiligo .
Pregnant or lactating women. History of keloid formation. Hematological disorders coagulopathies, or use of anticoagulant therapy or medications that may prolong bleeding Previous vitiligo treatment in the last 2 months.
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