- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01122095
Cross-sectional Evaluation of Biological Markers of Cardiovascular Disease in Children and Adolescents With Psoriasis
Hypothesis 1: Patients with psoriasis will have clinical and laboratory assessments differing from control patients.
Hypothesis 2: Patients with psoriasis will have laboratory alterations that correlate with other clinical characteristics of their psoriasis.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
California
-
San Diego, California, United States, 92123
- Recruiting
- Rady Children's Hospital Dermatolgoy
-
Contact:
- Donna Pascual, LVN
- Phone Number: 4295 858-576-1700
- Email: dpascual@rchsd.org
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Contact:
- Ann Funk, RN, CCRC
- Phone Number: 4295 858-576-1700
- Email: afunk@rchsd.org
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Sub-Investigator:
- Wynnis Tom, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Subjects of any race or ethnicity who meet all of the following criteria are eligible for enrollment into the study:
- The subject has a diagnosis of typical psoriasis, with or without arthritis, based on the clinical evaluation by an investigator or a prior diagnosis by a pediatric dermatologist
- Persons residing in the US.
- Subjects 0 to 18 years of age.
- Subjects/Guardians willing and able to comply with the requirements of the study.
- Subjects/Guardians willing and able to give informed consent.
- The subject is in general good health in the opinion of the investigator.
Exclusion Criteria:
- Over 18 years of age.
- Subject has had a diagnosis of congenital heart disease.
- Subject has had any cardiac catheterizations or surgeries.
- Subject has taken any cardiac medications (calcium channel blockers, beta blockers, vasotropic medicines) within the past 2 years.
- Subjects determined to have atypical psoriasis or isolated palmoplantar psoriasis.
- Subject diagnosed with any other systemic inflammatory disease including atopic dermatitis, severe acne vulgaris, inflammatory bowel disease, juvenile idiopathic arthritis, connective tissue disease and other similar conditions.
- Having autoimmune or immunodeficiency disease.
- Presence of active systemic fungal, bacterial, or viral infections.
- Presence of active systemic malignancy.
- Mental illness or history of drug or alcohol abuse that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements.
- Inability or unwillingness of a participant to give written informed consent.
Control Inclusion Criteria:
- Age up to 18 years.
- Ability and willingness to provide informed consent.
Control Exclusion Criteria:
- Over 18 years of age.
- Subject has had a diagnosis of congenital heart disease.
- Subject has had any cardiac catheterizations or surgeries.
- Subject has taken any cardiac medications (calcium channel blockers, beta blockers, vasotropic medicines) within the past 2 years.
- Subjects determined to have psoriasis of any type or a family history (first degree relative) with psoriasis.
- Subject diagnosed with any other systemic inflammatory disease including atopic dermatitis, severe acne vulgaris, inflammatory bowel disease, juvenile idiopathic arthritis, connective tissue disease and other similar conditions.
- Having autoimmune or immunodeficiency disease.
- Presence of active systemic fungal, bacterial, or viral infections.
- Presence of active systemic malignancy.
- Mental illness or history of drug or alcohol abuse that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements.
- Inability or unwillingness of a participant to give written informed consent.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Psoriasis
Children with psoriasis Age matched controls without psoriasis or other significant inflammatory disease
|
Control patient
Age matched, without psoriasis or significant inflammatory disease
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Obesity risk assessment
Time Frame: 6 months
|
Body Mass Index; C-reactive protein (CRP)
|
6 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Lawrence F. Eichenfield, MD, University of Calfornia, San Diego
Publications and helpful links
General Publications
- 1. Neimann AL, Shin DB, Wang X, Margolis DJ, Troxel AB , Gelfand JM. Prevalence of cardiovascular risk factors in patients with psoriasis. J Am Acad Dermatol 2006;55:829-35. 2. Gelfand J, Neimann A, Shin D et al. Risk of myocardial infarction in patients with psoriasis. JAMA. 2006;296:1735-1741. 3. Gelfand J, Troxel B, Lewis J et al. The risk of mortality in patients with psoriasis: Results from a population-based study. Arch Dermatol. 2007;143(12):1493-1499 4. Kelishadi R, Ardalan G, Gheiratmand R, Adeli K, Delavari A, and Majdzadeh R et al. Pediatric metabolic syndrome and associated anthropometric indices: the CASPIAN study. Acta Paediatrica, 2006. 95: 1625-1634. 5. Goodman E, Dolan L, Morrison J and Daniels S. Factor Analysis of Clustered Cardiovascular Risks in Adolescence. Circulation 2005; 111: 1970-1977. 6. Schwimmer JB, Pardee PE, Lavine JE, Blumkin AK, Cook S. Cardiovascular Risk Factors and the Metabolic Syndrome in Pediatric Nonalcoholic Fatty Liver Disease. Circulation. 2008 June. 118:277-283.
Study record dates
Study Major Dates
Study Start
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20080414
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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