Comparative Study of Microneedling With Topical Minoxidil 5% ± NB-UVB in Stable Vitiligo"

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age16-60
SponsorSohag University

About this trial

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

Eligibility criteria

Qualifiers

Patients with stable non-segmental vitiligo

No new lesions

No enlargement of existing lesions

Patients of both sexes

Disqualifiers

Active vitiligo

Pregnant or lactating women

History of keloid formation

Hematological disorders

Trial design

Treatments tested in this trial

  • microneedling with minoxidil 5% and NBUVB
  • Microneedling with Minoxidil5%

Treatment groups

30 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators