Alopecia Areata
Conditions
Keywords
Alopecia areata, Excimer, UVB
Brief summary
Alopecia Areata (AA) is a chronic autoimmune inflammatory disease causing nonscarring hair loss. Many treatment modalities have been found to be helpful in AA, however, none on them cure the disease. UVB excimer light has recently emerged as a new therapeutic modality in many dermatologic diseases. There are no prospective randomized controlled trials evaluating the efficacy and safety of UVB excimer light in AA. We plan on conducting a prospective split lesion single-blinded randomized clinical trial to assess efficacy and safety of UVB excimer light in the treatment of AA.
Detailed description
Alopecia Areata (AA) is a chronic autoimmune inflammatory disease causing nonscarring hair loss. Many treatment modalities have been found to be helpful in AA, however, none on them cure the disease. Excimer laser has been shown to be effective in the treatment of AA in controlled studies. The main disadvantage of the previous studies evaluating excimer laser is choosing separate patches as a control which does not account for interlesional treatment response variability. UVB excimer light has recently emerged as a new therapeutic modality in many dermatologic diseases. However, there are only a few studies that evaluated the efficacy and safety of UVB excimer light in AA. Those studies have shown that UVB excimer light is effective in the treatment of AA but none of them was conducted in a controlled fashion. There are no prospective randomized controlled trials evaluating the efficacy and safety of UVB excimer light in AA. We plan on conducting a prospective split lesion single-blinded randomized clinical trial to assess efficacy and safety of UVB excimer light in the treatment of AA. Study Objectives 1. To evaluate the potential for UVB excimer light to induce hair regrowth within AA patches. 2. To assess the side effect profile of UVB excimer light when used in the treatment of AA.
Interventions
PROCEDUREUVB excimer light
Sponsors
University of British Columbia
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age \> 18 years. * Subject has a patch of at least 12 cm2 on the scalp with no evidence of hair regrowth. * Subject is willing and capable of cooperating to the extent and degree required by the protocol.
Exclusion criteria
* Patients who received treatment for alopecia areata within the past 4 weeks. * Patients with alopecia totalis or alopecia universalis. * Patients with known photosensitivity like having polymorphous light eruption, connective tissue diseases, porphyria or Xeroderma pigmentosum. * Pregnancy or breast-feeding. * History of previous skin cancer. * Patients that have participated in another investigational drug or device study within 30 days of enrollment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in the percentage of hair regrowth for each half. We will consider the treamtment successful if there was ≥50% hair regrowth from baseline. | at 6, 12, and 16 weeks from baseline |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of side effects in each half | at 6, 12, and 16 weeks from baseline |
| Change in hair count and caliber in each half | at 6, 12, and 16 weeks from baseline |
Countries
Canada
Contacts
Primary ContactHarvey Lui, MD, FRCPC
Outcome results
None listed