Study Summary
This trial will test whether UVA1 phototherapy is an effective and safe treatment for vitiligo.
Treatment Effectiveness
Effectiveness Progress
Study Objectives
1 Primary · 1 Secondary · Reporting Duration: assessments at 2, 4, 6, and 8 weeks during treatment then at 4, 8, and 12 weeks post treatment
Week 12
Assessment of side effects in each half including erythema, pruritus, and polymorphous light eruption
Change in the modified VASI score compared to baseline.
Trial Safety
Safety Progress
This is further along than 68% of similar trials
Trial Design
2 Treatment Groups
No treatment (covered)
1 of 2
UVA1
1 of 2
Active Control
16 Total Participants · 2 Treatment Groups
Primary Treatment: UVA1 · No Placebo Group · Phase 2
No treatment (covered)NoIntervention Group · 1 Intervention: No treatment (covered) · Intervention Types:
UVA1
Procedure
ActiveComparator Group · 1 Intervention: UVA1 · Intervention Types: ProcedureTrial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: assessments at 2, 4, 6, and 8 weeks during treatment then at 4, 8, and 12 weeks post treatment
Who is running the clinical trial?
University of British ColumbiaLead Sponsor
1,325 Previous Clinical Trials
1,534,077 Total Patients Enrolled
4 Trials studying Vitiligo
109 Patients Enrolled for Vitiligo
Harvey Lui, MD, FRCPCPrincipal InvestigatorUniversity of British Columbia
3 Previous Clinical Trials
64 Total Patients Enrolled
3 Trials studying Vitiligo
64 Patients Enrolled for Vitiligo
Eligibility Criteria
Age 18+ · All Participants · 3 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You have localized or generalized vitiligo that involves a non mucosal or acral site.
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Conditions
Cancer Related
Treatments