Blue Light Phototherapy
Primary Purpose
Grover's Disease, Psoriasis Vulgaris
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Blue light phototherapy
Sponsored by
About this trial
This is an interventional treatment trial for Grover's Disease
Eligibility Criteria
Inclusion Criteria:
- Patient's aged 18-89 at time of enrollment
- Previous diagnosis of psoriasis vulgaris or Grover's disease
Exclusion Criteria:
- 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.
Sites / Locations
- Northwestern University Department of Dermatology
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Adult treatment arm
Arm Description
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.
Outcomes
Primary Outcome Measures
Efficacy of Blue Light Therapy for Patients With Grover's Disease
Demonstrate preliminary skin efficacy as measured by lesion count
Assess User Experience With the Dermatology Life Quality Index (DLQI) Pre and Post-treatment.
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT04343586
First Posted
January 24, 2020
Last Updated
February 21, 2023
Sponsor
Northwestern University
Collaborators
T-Cellerate LLC
1. Study Identification
Unique Protocol Identification Number
NCT04343586
Brief Title
Blue Light Phototherapy
Official Title
Development & Preliminary Clinical Validation Blue Light Phototherapy Systems for T-Cell
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
December 20, 2021 (Actual)
Study Completion Date
September 22, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
Collaborators
T-Cellerate LLC
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will use Blue-light Photo-therapy to treat patients with psoriasis vulgaris and Grover's Disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Grover's Disease, Psoriasis Vulgaris
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Adult treatment arm
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
Blue light phototherapy
Other Intervention Name(s)
DusaPharma Blu-U model 4170
Intervention Description
Phototherapy- Wavelength: 417±15 nm
Primary Outcome Measure Information:
Title
Efficacy of Blue Light Therapy for Patients With Grover's Disease
Description
Demonstrate preliminary skin efficacy as measured by lesion count
Time Frame
Time Frame: 5 weeks
Title
Assess User Experience With the Dermatology Life Quality Index (DLQI) Pre and Post-treatment.
Description
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.
Time Frame
Time Frame: 5 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient's aged 18-89 at time of enrollment
Previous diagnosis of psoriasis vulgaris or Grover's disease
Exclusion Criteria:
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shuai Xu
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University Department of Dermatology
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Blue Light Phototherapy
We'll reach out to this number within 24 hrs