Stable Vitiligo Clinical Trial
Official title:
The Efficiency of Fractional-Laser Resurfacing Followed by Topical Tacrolimus 0.03% Cream Versus Topical Tacrolimus Alone in Stable Vitiligo: a Comparative Study
The aim the clinical trial was to find out whether fractional CO₂ laser sessions in combination with application of daily topical tacrolimus 0.03% would enhance the action of the drug and pose as a possible combination treatment option for stable vitiligo lesions. This combination treatment was applied to one side of the body and the response was compared to the response of the lesions on the other side of the body to daily topical tacrolimus 0.03% alone, which was used as control.
Each patient included in the study received treatment A on the lesions on one side of his/her
body, and treatment B on the other side.
Treatment A included 4 monthly sessions of fractional CO₂ laser on the lesions plus
application of topical tacrolimus 0.03% (Tarolimus) on the lesions 6 hours after each session
and twice daily in between the sessions and for 1 month after the last session.
Treatment B included only the application of topical tacrolimus 0.03% (Tarolimus) on the
lesions twice daily for 5 months.
Fractional laser The device used was DEKA, SmartXide DOT (Dermal Optical Thermolysis), Italy
fractional Carbon Dioxide Laser (fig. 8). This device is an ablative fractional 10,6000 nm
CO² Laser with variable pulse duration (0.2-2 ms), 350-μm beam spot size, scanner area of
15x15 mm and penetration depth between 200 to 1,500 μm.
Tacrolimus ointment 0.03% (Tarolimus) Applied on the lesions treated by fractional CO² laser
6 hours after each laser session, then twice daily in between the sessions and 1 month after
the last session.
Applied on the lesions on the other half of the body (not treated with fractional CO² laser)
twice daily for 4 months.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01701648 -
Melanocyte Transplantation for Patients With Stable Vitiligo.
|
Phase 1/Phase 2 |