Psoriasis
Conditions
Keywords
videocapillaroscopy, psoriasis, systemic agent
Brief summary
The aim of this study is to determine if videocapillaroscopy could be used as an objective and reliable method to assess psoriasis severity and to document improvement during treatment by measuring changes in vascular features.
Detailed description
This is a single-center, prospective, observational study that will recruit subjects from Northwestern University to examine the degree of improvement of psoriatic plaques during systemic therapy treatment. Thirty patients with a confirmed diagnosis of active psoriasis treated with a single systemic agent will be recruited from the Northwestern Medical Faculty Foundation Dermatology clinic. The study population will include 15 patients receiving adalimumab and 15 patients receiving methotrexate. Eight visits will be completed for each subject: visit 0 (baseline) and visits 1-8 (week 2, 4, 6, 8, 12, 16 and 24). At the baseline visit, after informed consent is obtained, a capillaroscopic examination will be performed to assess for evidence of characteristic vascular alterations. If such changes are present, the remainder of the baseline visit will be completed. This includes gathering personal information (age, race, gender etc.), clinical history (time of first diagnosis, presentation site, treatment used, biopsy results if previously performed, etc.) and past medical history (including current and previous medications). At each of the subsequent visits (visit 1-8), any changes to medical history and/or medications will be obtained and recorded. At each of the eight visits, a dermatologic physical examination, including PASI and PGA scores will be performed.
Interventions
None listed
Sponsors
AbbVie
Northwestern University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Subjects with a clinical diagnosis of chronic active plaque psoriasis * Subjects eligible for systemic monotherapy (oral or biologic agents). * Subjects with evidence of characteristic vascular alterations on capillaroscopic examination. * Subjects who are able to complete the study visits and procedures, including completion of the DLQI questionnaire. * Subjects who are willing to have standardized digital photographs taken of 2 different target plaque lesions on the extremities. * Subjects who are willing to have videocapillaroscopic photographs taken of 2 different target plaque lesions as well as of 2 areas of uninvolved skin on the extremities. * Subjects who have had a 4 week washout period if they have recently changed systemic psoriatic therapy.
Exclusion criteria
* Those who do not fit the inclusion criteria. * Subjects who are unable to understand the protocol or give informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Videocapillaroscopy assessment in psoriasis | Week 0, 2, 4, 6, 8, 12, 16 and 24 | The primary objective is to determine if videocapillaroscopy could be used as an objective and reliable method to assess psoriasis severity and to document improvement during treatment by measuring changes in vascular features. |
Countries
United States
Outcome results
None listed