Vitiligo Clinical Trial
Official title:
Efficacy of Red Light in Vitiligo: A Prospective, Single-Blind Randomized Controlled Trial
NCT number | NCT01787708 |
Other study ID # | H10-02235b |
Secondary ID | |
Status | Recruiting |
Phase | Phase 2 |
First received | February 4, 2013 |
Last updated | June 30, 2015 |
Start date | February 2013 |
Vitiligo is a chronic acquired disease characterized by well defined white macules and patches affecting the skin. There are many treatment modalities available for vitiligo, however, none of them cure the disease. Visible red light has been shown to stimulates melanocyte migration and proliferation resulting in repigmentation of vitiligo patches. However, there are only a few studies published on the efficacy of red light in vitiligo. This is a prospective single-blind randomized clinical trial to assess efficacy of red light in the treatment of vitiligo.
Status | Recruiting |
Enrollment | 16 |
Est. completion date | |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - Age > 18 years. - Localized or generalized vitiligo that involves a non mucosal or acral site. - Patients should have a patch of at least 25 cm2 that shows no more than 10% repigmentation as assessed visually Exclusion Criteria: - Patients who received treatment for vitiligo within the past 3 weeks. - Patients known to have a photosensitivity disorder - History of previous skin cancer. - History of severe medical illness or immunosuppression. - Pregnancy or breast-feeding. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | The Skin Care Center, Vancouver General Hospital | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
University of British Columbia |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in the modified VASI score compared to baseline. | assessments at 2, 4, 6, 8 and 10 weeks during treatment then at 4, 8, and 12 weeks post treatment | No |
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