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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00115232
Other study ID # 04-03-044
Secondary ID
Status Completed
Phase N/A
First received June 21, 2005
Last updated January 14, 2008
Start date July 2004
Est. completion date March 2007

Study information

Verified date January 2008
Source Children's Hospital Boston
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate levels of inflammatory mediators in children at risk for cardiovascular disease due to family history. We are measuring inflammatory markers in two groups of children and their parents: children with a family history of early atherosclerotic heart disease (cases), and healthy children without such a family history (controls). The design is a cross-sectional study, gathering a fasting blood sample and clinical and behavioral data on children and a parent.


Description:

Family history is a well known risk factor for early atherosclerosis. Whether inflammation plays a role in the increased risk of family history is not known. In this prospective single-center study, we are recruiting children with and without a family history of premature atherosclerotic disease, defined as occurring < 55 years in males and <65 years in females. Children are recruited primarily from a pediatric preventive cardiology clinic at Children's Hospital Boston. We measure anthropomorphic characteristics, fasting lipid profiles and inflammatory marker levels, including high sensitivity C-reactive protein (hsCRP), intracellular adhesion molecule 1 (ICAM-1), P-selectin, and tumor necrosis factor alpha receptor 2 (TNFαR2).

In this sample of high-risk overweight children, Lp(a) and inflammatory markers could reflect cardiovascular risk outside lipid profiles.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 2007
Est. primary completion date October 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 8 Years to 21 Years
Eligibility Inclusion Criteria:

- Age 8-21 years

- Parent able to participate

- Fasting state

- Live locally

Exclusion Criteria:

- Taking medication that may alter cholesterol levels or inflammatory state

- Past or present inflammatory illnesses

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
United States Children's Hospital Boston Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Children's Hospital Boston Sandra A. Daugherty Foundation

Country where clinical trial is conducted

United States, 

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