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Interest of the Dermabrasion by Laser Erbium in the Treatment of the Vitiligo

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01087216
Enrollment
20
Registered
2010-03-16
Start date
2010-03-31
Completion date
2011-03-31
Last updated
2012-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitiligo

Brief summary

The treatment of vitiligo remains disappointing especially in some localization such as bony prominences and extremities. The association of UVB and topical steroids has been proven to be synergistic but the results are still insufficient in those difficult to treat areas. Promising results have been shown with the combination of laser assisted dermabrasion, topical 5FU and UVB. The investigators hypothesize that the dermabrasion of vitiligo skin followed by topical steroids should potentialized the effect of UVB and be superior to topical steroids and UVB without dermabrasion. The main objective of this study is to evaluate the usefulness of laser assisted dermabrasion combined to topical steroids and UVB phototherapy in difficult to treat areas. Patients with symmetrical non segmental vitiligo will be included in this prospective randomized monocentrer study. The investigators calculated the number of patients needed at 25. The side that will receive the dermabrasion will be centrally randomized and the opposite side will serve as control. Then on both side class 3 topical steroids will be applied daily 3 weeks on 4 for 12 weeks. UVB phototherapy will be performed twice weekly also for 12 weeks. The evaluation will be performed by two independent physician blinded to the treatment of standardized photos before and 1 month after the end of the treatment. The criteria of success will be at least 75% of repigmentation.

Interventions

DEVICEGroup Laser = Arm A

Opposite side lesions that will receive only the treatment by topical steroids and UVB phototherapy

DRUGBras B : The group control

patient to accept habitual treatment of corticoid Opposite side lesions that will receive only the treatment by topical steroids

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 at 85 * Not segmental Vitiligo of clinical diagnosis located on bony projections or of ends * Two symmetrical plates of vitiligo of more than 4 cm ²

Exclusion criteria

* Pregnant women or breastfeeding. * Vitiligo lesions on face and neck * Personal history of skin cancer * Photosensitize drugs * Personal history of photodermatosis * Personal history of keloids * Concomitant treatment that could have an action on vitiligo (such as tacrolimus or pimecrolimus).

Design outcomes

Primary

MeasureTime frameDescription
Lesions that will receive the treatment by dermabrasion associate to habitual treatment of topical steroids and UVB phototherapy4 monthsOpposite side lesions that will received only the treatment by topical steroids and UVB phototherapy

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026