ClinicalTrials.Veeva

Menu

Transplantation of Basal Cell Layer Suspension Using Derma-rolling System in Vitiligo

M

Mohammed V University of Rabat

Status

Unknown

Conditions

Vitiligo

Treatments

Device: Dermabrasion with dermaroller

Study type

Interventional

Funder types

Other

Identifiers

NCT02962180
MOHAMMED V UNIVERSITY

Details and patient eligibility

About

Actually the methods for melanocyte delivery are invasive and often sophisticated. The dermarolling system with needles causing tiny microinjuries in the epidermis could offer a minimally invasive and painless method of melanocyte transplantation. The purpose of the study is to develop a new and simple method for transepidermally delivering keratinocytes and melanocytes into vitiligo skin.

Full description

Condition: stable lesion of non segmental and segmental vitiligo of adults.

Background: The best method to transepidermally deliver isolated cells (melanocytes) is not yet defined. Microneedle treatment of the " ex vivo " human skin caused many thin vertical epidermodermal fissures and a variable depth of injury into the dermis regarding the length of the needles. This kind of treatment could be able to create small epidermal defects which allows to deliver melanocytes to an epidermal site. An approach to replenish melanocytes by injection of dissociated epidermal cell suspension with a syringe was recently successfully used. So, we hypothesize that the use of dermaroller with 0.2mm needle length which causes tiny microinjuries strictly in the epidermis could offer a simple, minimally invasive and painless method of melanocyte transplantation.

Main objective: To demonstrate the efficacy and the interest of dermaroller use with 0.2mm needle length in the transplantation of basal cell layer suspension in the epidermis of depigmented vitiligo skin.

Secondary objectives

  1. To assess as control the effect of the use of dermaroller alone on the vitiligo lesion.
  2. If transplantation is successful, to assess the duration needed to obtain a good coalescence and a complete repigmentation of the vitiligo lesion.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Non segmental and segmental vitiligo lesions stable for a minimum of 1 year prior surgery
  • Men and women aged over 18 years of age
  • The lesion area must be 2cm2< lesion< 15cm2
  • Absence of infected lesion

Exclusion criteria

  • Actively spreading vitiligo (unstable disease)
  • Patient with history of melanoma
  • Infected lesions
  • Positive Koebner Phenomenon
  • History of hypertrophic scars or keloid formation
  • Treatment with immunosuppressive or cytotoxic medication the past year
  • Pregnant women and patients aged less 18 years
  • Patients with concomitant photosensitizing treatment
  • Positive serology of herpes, HIV, hepatitis B and C

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

single arm study
Experimental group
Description:
Dermabrasion with dermaroller of basal cell layer suspension obtained by soft trypsinisation in vitiligo lesion.
Treatment:
Device: Dermabrasion with dermaroller

Trial contacts and locations

1

Loading...

Central trial contact

laila benzekri, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems