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Relationship Between Functional Health Status and Ventricular Performance After Fontan (A Trial Conducted by the Pediatric Heart Network) - Article


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Congenital bilateral absence of vas deferens

Absence of vas deferens; Absent vasa; CAVD; CBAVD


Clinical Trial: Relationship Between Functional Health Status and Ventricular Performance After Fontan (A Trial Conducted by the Pediatric Heart Network)

This study has been completed.

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier: NCT00132782

Purpose

The purpose of this cross-sectional study was to determine the interrelationships between health status and measures of cardiac performance in children 6 to 18 years of age with congenital heart disease who have undergone a Fontan procedure as surgical treatment for functional single ventricle. The goal was to develop a data set that will permit identification of a clinically relevant endpoint for subsequent trials of medical management of the Fontan patient.
Condition
Defect, Congenital Heart
Arrhythmia

MedlinePlus related topics:  Arrhythmia;   Congenital Heart Disease

Study Type: Observational
Study Design: Natural History, Cross-Sectional

Further Study Details: 

Study start: March 2003;  Study completion: February 2004

BACKGROUND:

Children born with one functional ventricle and who undergo a Fontan procedure, have a higher incidence of late complications than other congenital heart patients. While the Fontan procedure results in restoring near-normal systemic oxygen saturation, there are recognized problems and little information about the overall health status, functional status and ventricular performance in these children.

DESIGN NARRATIVE:

This cross-sectional observational study included children 6-18 years of age who had undergone a Fontan procedure for a congenital cardiac defect. Prospective data collection for each patient occured within a 3 month time period and included cardiac MRI, echocardiography, serology and exercise testing. Historical clinical and surgical data, as well as parent and child self reports of health status, was collected.

Eligibility

Genders Eligible for Study:  Both
Criteria
No eligibility criteria

More Information

Study ID Numbers:  242
Last Updated:  August 19, 2005
Record first received:  August 19, 2005
ClinicalTrials.gov Identifier:  NCT00132782
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-08-23


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October 10, 2008



Page Updated: September 6, 2005
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