Characterization of Lipoprotein Composition and Function in Pediatric Psoriasis Before and After Treatment
Status: | Recruiting |
---|---|
Conditions: | Psoriasis |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 6 - 17 |
Updated: | 1/3/2019 |
Start Date: | December 1, 2018 |
End Date: | December 2020 |
Contact: | DermatologyCTU |
Email: | NUderm-research@northwestern.edu |
Phone: | 312-503-5944 |
This study will assess differences in inflammatory proteins, lipoprotein composition,
cholesterol efflux and HDL-proteome in moderate-to-severe pediatric psoriasis who at baseline
begin systemically administered therapy vs: a) healthy controls; and b) patients with milder
psoriasis.
cholesterol efflux and HDL-proteome in moderate-to-severe pediatric psoriasis who at baseline
begin systemically administered therapy vs: a) healthy controls; and b) patients with milder
psoriasis.
Inclusion Criteria:
- Children ages 6-17 years of all races/ethnicities with plaque and/or extensive guttate
psoriasis for at least 6 months and on topical or systemic therapy
- Patients in the systemic group can be starting a medication for the first time OR
transitioning from another systemic if unresponsive and on that previous treatment for
≤ 3 months.
- Patients may concurrently have psoriatic arthritis if initiation of a systemic
medication is warranted by skin severity.
- Children ages 6-17 years of all races/ethnicities with acne being treated with
isotretinoin
- Children ages 6-17 years of all races/ethnicities without plaque or guttate psoriasis
and history of severe acne or treatment with isotretinoin as controls.
Exclusion Criteria:
- Patients less than 6 years of age or 18 years and older
- Patients with congenital heart disease, prior cardiac catheterizations/surgeries, or
on cardiac medications in the past two years other than for hypertension (eg, calcium
channel-blockers, beta-blockers and vasotropic medications).
- Patients who have other systemic inflammatory diseases (including atopic dermatitis,
severe acne, inflammatory bowel disease, juvenile idiopathic arthritis, connective
tissue diseases and/or other autoimmune diseases).
- Patients who have active infection or malignancy or have suffered from infection
requiring oral or parenteral antibiotic in past 2 weeks.
- Patients and parents/caregivers unable to give written informed consent.
We found this trial at
1
site
225 E Chicago Ave
Chicago, Illinois 60611
Chicago, Illinois 60611
(312) 227-4000
Principal Investigator: Amy Paller, MD
Phone: 312-503-5944
Ann & Robert H. Lurie Children's Hospital of Chicago Ann & Robert H. Lurie Children
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