Condition: Vitiligo · Sponsor: Hospital Authority, Hong Kong
This trial is a prospective, open-label, single-center, split face randomized controlled study comparing 1.5% topical Ruxolitinib cream twice daily (BD) to aqueous cream in treating non-segmental vitiligo (NSV) of the face and neck in patient previous failed to respond to topical tacrolimus 0.1%. Aqueous cream twice daily application will be used as control group treatment. Patients with stable NSV at least 0.5% of their total body surface area (BSA) on the face and neck, as determined by the fingertip method, are screened. Recruited subjects will be asked to review their impression of change of their lesion by the end of the study using a 7-point scale.
This description comes directly from the study's public registry record.
Research Assistant · +85222555885 · js83213@hku.hk
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| Queen Mary Hospital, Hospital Authority | Hong Kong, Hong Kong | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06719024