Blue Light Phototherapy
- Conditions
- Psoriasis VulgarisGrover's Disease
- Interventions
- Device: Blue light phototherapy
- Registration Number
- NCT04343586
- Lead Sponsor
- Northwestern University
- Brief Summary
This study will use Blue-light Photo-therapy to treat patients with psoriasis vulgaris and Grover's Disease.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 11
- Patient's aged 18-89 at time of enrollment
- Previous diagnosis of psoriasis vulgaris or Grover's disease
-
All Groups: Subjects who are younger than 18 years of age or older than 90 years of age
-
Patients who have received topical or systemic treatment within the prior 2 weeks of planned phototherapy
-
Patients prescribed any of the following drugs for issues not related to their psoriasis or Grover's disease
- topical steroids
- calcineurin inhibitors
- methotrexate
- retinoids
- biologic agents
-
Unable to schedule phototherapy sessions
-
We will not recruit the following populations: adults unable to consent, individuals who are not yet adults (infants, children, teenagers), pregnant women, prisoners and other vulnerable populations.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Adult treatment arm Blue light phototherapy Adults enrolled in the study will receive treatment (blue light phototherapy) on one area of their body affected by psoriasis or Grover's disease. The treatment area (restricted by size of the device) will be compared to untreated areas affected by disease on the same patient.
- Primary Outcome Measures
Name Time Method Assess User Experience With the Dermatology Life Quality Index (DLQI) Pre and Post-treatment. Time Frame: 5 weeks The DLQI is a questionnaire with 10 questions. The maximum score is 30 and minimum is 0. The higher the score, the more quality of life is impaired.
Efficacy of Blue Light Therapy for Patients With Grover's Disease Time Frame: 5 weeks Demonstrate preliminary skin efficacy as measured by lesion count
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Northwestern University Department of Dermatology
🇺🇸Chicago, Illinois, United States