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Not yet recruiting Phase 2 NCT07548918

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: БГ
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. \-
Interventions
microneedling with minoxidil 5% and NBUVB
COMBINATION_PRODUCT
Microneedling with Minoxidil5%
COMBINATION_PRODUCT
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Phase 2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
16 Years
Maximum age
60 Years
Healthy volunteers
No
Start date
20.05.2026
Completion date
15.10.2027
Registry ID
NCT07548918
Source
clinicaltrials.gov
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