Skip to main content
OpenTrials
Completed

NCT Number: NCT00930592

Peds Metabolic Syndrome in Psoriasis

The objective of this study is to assess whether there is an increased risk of the metabolic syndrome in children with psoriasis compared to children without psoriasis.

Completed

Looking for future studies?

Notify Me

Key information

Age range

10 year–17 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Tufts Medical Center, Department of Dermatology

Boston, Massachusetts, 02111, United States

About this study

Adult patients with psoriasis, especially those who are young and with severe disease, have an increased prevalence of myocardial infarction and metabolic syndrome, and increased mortality. Tumor Necrosis Factor (TNF) and other inflammatory cytokines are felt to play an important role not only in the pathogenesis of psoriasis and psoriatic arthritis, but in the pathogenesis of the metabolic syndrome and increased cardiovascular mortality and morbidity.

However, the prevalence of metabolic syndrome and surrogate markers of increased cardiovascular risk, such as lower flow-mediated dilation (FMD) during reactive hyperemia, measured by high-resolution brachial artery ultrasound, lower hyperemia-induced, pulse wave amplitudes as measured by finger plethysmograph peripheral artery tonometry, and elevated blood CRP levels, in children with psoriasis, are unknown.

We will use the definition of metabolic syndrome described by de Ferranti: Participants are defined as having metabolic syndrome if they meet or exceed the criteria for 3 or more of the following 5 variables: 1) triglycerides ≥1.1 mmol/L; 2) HDL cholesterol <1.3 mmol/L; 3) fasting blood glucose ≥6.1 mmol/L; 4) waist circumference (cm) >75th percentile for age and sex; and 5) systolic or diastolic blood pressure (mm Hg) >90th percentile for age, sex, and height.

The following two noninvasive procedures will be used to assess additional cardiovascular risk: flow mediated dilation (FMD) and finger plethysmography peripheral artery tonometry (PAT). These procedures have been used extensively to measure adults for clinical study purposes for many years.

As a control group, we will compare children with psoriasis to age-, race-,and gender-matched children with warts.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 10-17 year old children with either moderate to severe psoriasis or with warts
  • For psoriasis patients, body surface area covered must be 5% or more or must have had a documented history of 5% or more body surface area involvement
  • Ability to understand and sign an age-appropriate consent form
  • Parent or Guardian over 18 years old able to understand and sign consent form

Exclusion criteria

  • Psoriasis or wart patient younger than 10 or 18 years or older
  • For psoriasis patients, body surface area covered less than 5% or have not had a documented history of 5% or more body surface area involvement
  • Inability of child or adult parent/guardian to understand or sign consent
  • Pregnant or lactating females.

Treatment and study plan

Primary outcomes

  1. The primary objective of this study is to determine if children with psoriasis will have an increased prevalence of the metabolic syndrome.

    Time frame: one assessment

Secondary outcomes

  1. Metabolic syndrome in children with psoriasis will be determined using body weight, BMI, waist circumference, blood pressure, fasting blood sugar, and blood lipid profile.

    Time frame: one assessment

  2. Surrogate endpoints indicating potential increased cardiovascular risks, including high sensitivity CRP, flow-mediated dilation (FMD) during reactive hyperemia, and hyperemia-induced, pulse wave amplitudes.

    Time frame: one assessment

  3. For psoriasis patients only: PASI, BSA, and PGA will be measured to establish extent of disease.

    Time frame: one assessment

  4. Safety Outcome Measures: All adverse events (AEs) will be recorded and monitored.

    Time frame: each occurance

Sponsors and collaborators

Lead sponsor

Tufts Medical Center

Other

Collaborators

  • Amgen

Registry information

Official study title

Assessor-Blinded Study of the Metabolic Syndrome and Surrogate Markers of Increased Cardiovascular Risk in Children With Moderate to Severe Psoriasis Compared With Age Matched Population of Children With Warts

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jun 30, 2009
Registry last updated
Apr 16, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.